Human serum albumin: twenty-three genetic variants and their population distribution
dc.contributor.author | Weitkamp, Lowell R. | en_US |
dc.contributor.author | Salzano, Francisco M. | en_US |
dc.contributor.author | Neel, James V. | en_US |
dc.contributor.author | Porta, F. | en_US |
dc.contributor.author | Geerdink, R. A. | en_US |
dc.contributor.author | Tárnoky, A. L. | en_US |
dc.date.accessioned | 2010-04-01T15:31:06Z | |
dc.date.available | 2010-04-01T15:31:06Z | |
dc.date.issued | 1973-04 | en_US |
dc.identifier.citation | WEITKAMP, L. R.; SALZANO, F. M.; NEEL, J. V.; PORTA, F.; GEERDINK, R. A.; TÁRNOKY, A. L. (1973). "Human serum albumin: twenty-three genetic variants and their population distribution." Annals of Human Genetics 36(4): 381-392. <http://hdl.handle.net/2027.42/66001> | en_US |
dc.identifier.issn | 0003-4800 | en_US |
dc.identifier.issn | 1469-1809 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/66001 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4748758&dopt=citation | en_US |
dc.format.extent | 1676818 bytes | |
dc.format.extent | 3110 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | 1973 University College London and Blackwell Publishing Ltd | en_US |
dc.title | Human serum albumin: twenty-three genetic variants and their population distribution | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Genetics | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | †University of Michigan Medical School, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | *University of Rochester School of Medicine and Dentistry, Rochester, New York | en_US |
dc.contributor.affiliationother | †Universidade Federal do Rio Grande do Sul, PÔrto Alegre, Brazil | en_US |
dc.contributor.affiliationother | §Ospedale Civile, Sondrio, Italy | en_US |
dc.contributor.affiliationother | Academic Hospital, Utrecht | en_US |
dc.contributor.affiliationother | ¶Royal Berkshire Hospital, Reading | en_US |
dc.identifier.pmid | 4748758 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/66001/1/j.1469-1809.1973.tb00602.x.pdf | |
dc.identifier.doi | 10.1111/j.1469-1809.1973.tb00602.x | en_US |
dc.identifier.source | Annals of Human Genetics | en_US |
dc.identifier.citedreference | Arends, T., Gallango, M. L., Layrisse, M., Wilbert, J., Heinen, H. D. ( 1969 ). Albumin Warao: New typo of human alloalbuminemia. Blood, 33 414. | en_US |
dc.identifier.citedreference | Arends, T., Weitkamp, L. R., Gallango, M. L., Neel, J. V. & Schultz, J. ( 1970 ). Gene frequencies and microdifferentiation among the Makiritare Indians. II. Seven serum protein systems. Am. J. Hum. Genet., 22 526. | en_US |
dc.identifier.citedreference | Atal, P. R., Mital, V. P. & Kulshrestha, R. C. ( 1970 ). Heterogeneity of human serum albumin. Report of a case of bisalbuminemia. Ind. J. Med. Set., 12 797. | en_US |
dc.identifier.citedreference | Baisden, R., Conn, R. B. & Anido, V. ( 1969 ). Heterogeneity of human serum albumin. Report of two cases of bisalbuminemia. Am. J. Clin. Path., 51 760. | en_US |
dc.identifier.citedreference | Bennhold, H., Peters, H. & Roth, E. ( 1954 ). Über einen Fall von kompletter AnalbuminÄmie ohne wesentliche Klinische Krankheitszeichen. Deutsch Gesel. Inneremed., 60 630. | en_US |
dc.identifier.citedreference | Bonazzi, L. ( 1968 ). On a rare genetic variation of plasma albumin: bisalbuminemia. Clin. Chim. Acta, 20 362. | en_US |
dc.identifier.citedreference | Chen, S.-H., Giblett, E. R., Anderson, J. E. & Forsum, B. L. G. ( 1972 ). Genetics of glutamic-pyruvic transaminase: its inheritance, common and rare variants, population distribution and differences in catalytic activity. Ann. Hum. Genet. (Lond.), 35 401. | en_US |
dc.identifier.citedreference | Cooke, K. B., Cleghorn, T. E. & Lockey, E. ( 1961 ). Two new families with bisalbuminemia: An examination of possible links with other genetically controlled variants. Biochem. J., 81 39P. | en_US |
dc.identifier.citedreference | Efremov, G. & Braend, M. ( 1964 ). Serum albumin: Polymorphism in man. Science, N.Y., 146 1679. | en_US |
dc.identifier.citedreference | Emanuelli, G., Monni, A., Congiu, P., Palomba, V. & Pilleri, G. ( 1970 ). Bisalbuminemia of the fast type. Acta haemat., 44 246. | en_US |
dc.identifier.citedreference | Fine, J. M. ( 1970 ). Les allotypes de l'albumine humaine. Étude de 8 cas do bisalbuminÉmie observÉs en France. Rev. Europ. Etudes Clin. Biol., 15 113. | en_US |
dc.identifier.citedreference | Giblett, E. R. ( 1969 ). Genetic Markers in Human Blood, p. 456. Philadelphia : F. A. Davis. | en_US |
dc.identifier.citedreference | Gitlin, D., Schmid, K., Earle, D. P. & Givelber, H. ( 1961 ). Observations on double albumin. II. A peptide difference between two genetically determined human serum albumins. J. Clin. Invest., 40 820. | en_US |
dc.identifier.citedreference | Gordon, R. S., Jr., Bartter, F. C. & Waldmann, T. ( 1959 ). Idiopathic hypoalbuminemias. (Clinical Staff Conferences at the National Institutes of Health.) Ann. Int. Med., 51 553. | en_US |
dc.identifier.citedreference | Harris, H., Hopkinson, D. A., Luffman, J. E. & Rapley, S. ( 1968 ). Electrophoretic variation in erythrocyte enzymes. In Hereditary Disorders of Erythrocyte Metabolism, vol. ii ( ed. E. Beutler ), pp. 1 – 20. City of Hope Symposium Series. New York : Grune and Stratton. | en_US |
dc.identifier.citedreference | Jamieson, G. A. & Ganguly, P. ( 1969 ). Studies on a genetically determined albumin dimer. Biochem. Genet., 3 403. | en_US |
dc.identifier.citedreference | Knedel, M. ( 1957 ). Die Doppel-AlbuminÄmie, eine neue erbliche Proteinanomalie. Blut, 3 129. | en_US |
dc.identifier.citedreference | Kueppers, F., Holland, P. V. & Weitkamp, L. R. ( 1969 ). Albumin Santa Ana. A new inherited variant. Human Hered., 19 378. | en_US |
dc.identifier.citedreference | Lau, T., Sunderman, F. W. Jr., Agarwal, S. S., Sutnick, A. I. & Blumberg, B. S. ( 1969 ). Genetics of albumin Gainesville. A new variant of human serum albumin. Nature, Lond., 221 66. | en_US |
dc.identifier.citedreference | Lau, T. J., Sunderman, F. W. Jr., Weitkamp, L. R., Agarwal, S. S., Sutnick, A. I., Blumberg, B. S. & Carrillo de Jimenez, R. B. ( 1972 ). Albumin Cartago: a ‘new’ slow moving alloalbumin. Am. J. Clin. Path., 57 247. | en_US |
dc.identifier.citedreference | Laurell, C.-B. & NilÉhn, J.-E. ( 1966 ). A new type of inherited serum albumin anomaly. J. Clin. Invest., 45 1935. | en_US |
dc.identifier.citedreference | Lisker, R., Cobo, L. & Mora, G. ( 1971 ). Distribution of albumin variants in Indians and non-Indians of Mexico. Am. J. Phys. Anthrop., 35 119. | en_US |
dc.identifier.citedreference | Lie-Injo, L. E., Weitkamp, L. R., Kosasih, E. N., Bolton, J. M. & Moore, C. L. ( 1971 ). Unusual albumin variants in Indonesians and Malayan aborigines. Hum. Hered., 21 376. | en_US |
dc.identifier.citedreference | Margni, R. A., Heer, E. E., Acerbo, E., Hajos, S., Beliveau, M. & Bobbi, M. E. ( 1970 ). Immunochemical and genetic studies in two bisalbuminemic families. Clin. Chim. Acta, 29 219. | en_US |
dc.identifier.citedreference | McDermid, E. M. ( 1971a ). Serum albumin variation in Indian populations. Vox Sang., 21 462. | en_US |
dc.identifier.citedreference | McDermid, E. M. ( 1971b ). Variants in human serum albumin and caeruloplasmin in populations from Australia, New Guinea, South Africa and India. Aust. J. Exp. Biol. Med. Sci., 49 309. | en_US |
dc.identifier.citedreference | McDermid, E. M. & Vos, G. H. ( 1971 ). Serum protein groups of South African Indians. S. Afr. J. Med. Sci., 36 57. | en_US |
dc.identifier.citedreference | Melartin, L. ( 1967 ). Albumin polymorphism in man. Acta Path. Microb. Scand. Supplementum, 191 1. | en_US |
dc.identifier.citedreference | Melartin, L. & Blumberg, B. S. ( 1966 ). Albumin Naskapi: a new variant of serum albumin. Science, N.Y., 153 1664. | en_US |
dc.identifier.citedreference | Melartin, L., Blumberg, B. S. & Lisker, R. ( 1967 ). Albumin Mexico. A new variant of serum albumin. Nature, Lond., 215 1288. | en_US |
dc.identifier.citedreference | Melartin, L., Blumberg, B. S. & Martin, J. R. ( 1968 ). Albumin polymorphism (Albumin Naskapi) in Eskimoes and Navajos. Nature, Lond., 218 787. | en_US |
dc.identifier.citedreference | Neel, J. V. ( 1971 ). The detection of increased mutation rates in human populations. Perspect. Biol. Med., 14 522. | en_US |
dc.identifier.citedreference | Nennstiel, H. J. & Becht, T. ( 1957 ). Über das erbliche Auftreten einer Albuminspaltung im Elektrophorese diagramm. Klin. Wschr., 35 689. | en_US |
dc.identifier.citedreference | Polesky, H. F. & Rokala, D. A. ( 1967 ). Serum albumin polymorphism in North American Indians. Nature, Lond., 216 184. | en_US |
dc.identifier.citedreference | Polesky, H. F., Rokala, D. A. & Burch, T. ( 1968 ). Serum albumin polymorphism in Indians of the Southwestern United States. Cited in Weitkamp, Franglen et al. ( 1969 ). | en_US |
dc.identifier.citedreference | Porta, F., Ruffini, G., Ortali, V. & Fisauli, F. ( 1972a ). Alloalbuminemia. Analytical separation by electrophoretic procedure. Proc. Int. Symp. on Standardization in Haematology and Clinical Pathology, Sept. 1971, pp. 241 – 6. Foggia ( Italy ): S. Giovanni Rotondo. | en_US |
dc.identifier.citedreference | Porta, F., Ruffini, G., Pasino, M. & Scherini, A. ( 1972 ). Alloalbuminemia (bisalbuminemia) di tipo lento. Minerva Med., Roma, 63 1316. | en_US |
dc.identifier.citedreference | Robson, E. B. & Harris, H. ( 1967 ). Further studies on the genetics of placental alkaline phosphatase. Ann. Hum. Genet. (Lond.), 30 219. | en_US |
dc.identifier.citedreference | Rose, M., Blaszozyk, J. & Geserick, G. ( 1971 ). Eine humane Serumalbuminvariante (Doppelalbuminamie). Humangenetik, 11 132. | en_US |
dc.identifier.citedreference | Sandor, G., Martin, L., Porsin, M., Rousseau, A. & Martin, R. ( 1965 ). A new bisalbuminaemic family. Nature, Lond., 308 1222. | en_US |
dc.identifier.citedreference | Schultze, H. E. & Heremans, J. F. ( 1966 ). Molecular Biology of Human Proteins, vol. 1, p. 403. Amsterdam : Elsevier. | en_US |
dc.identifier.citedreference | TÁrnoky, A. L. & Dowding, B. ( 1969 ). Albumin Kashmir. A new variant and its behavior on routine analysis. Clin. Chim. Acta, 26 455. | en_US |
dc.identifier.citedreference | TÁrnoky, A. L. & Lestas, A. N. ( 1964 ). A new type of bisalbuminemia. Clin. Chim. Acta, 9 551. | en_US |
dc.identifier.citedreference | TÁrnoky, A. L., Dowding, B. & Lakin, A. L. ( 1970 ). Eight types of bisalbuminemia. Nature, Lond., 225 742. | en_US |
dc.identifier.citedreference | Ungari, S. & Lopez, V. ( 1965 ). Doppia albuminemia. Min. Pediat., 17 288. | en_US |
dc.identifier.citedreference | Weitkamp, L. ( 1971 ). Prospects for the automated typing of biochemical markers for the purpose of monitoring the human germinal mutation rate. In Monitoring, Birth Defects and Environment ( ed. E. B. Hook, D. T. Janerich and I. H. Porter ), p. 217. New York : Academic Press. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Arends, T., Gallango, M. L., Neel, J. V., Schultz, J. & Shreffler, D. C. ( 1972 ). The genetic structure of a tribal population, the Yanomama Indians. III. Seven serum protein systems. Ann. Hum. Genet. (Lond.), 35 271. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Basu, A., Gall, J. C. & Brown, W. ( 1969 ). Albumin Cayemite: a Negro plasma albumin variant. Humangenetik, 7 180. | en_US |
dc.identifier.citedreference | Weitkamp, L. R. & Buck, A. A. ( 1972 ). Phenotype frequencies for four serum proteins in Afghanistan: two ‘new’ albumin variants. Humangenetik, 15 335. | en_US |
dc.identifier.citedreference | Weitkamp, L. R. & Chagnon, N. A. ( 1968 ). Albumin MÁku. A new variant of human serum albumin. Nature, Lond., 217 759. | en_US |
dc.identifier.citedreference | Weitkamp, L., Chagnon, N., Saave, J., Salzano, F. & Gall, J. ( 1968 ). Serum albumin variants in American and New Guinea indigenes. Clin. Res., 16 298. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Franglen, G., Rokala, D. A., Polesky, H. F., Simpson, N. E., Sunderman, F. W. Jr., Bell, H. E., Saave, J., Lisker, R. & Bohls, S. W. ( 1969 ). An electrophoretic comparison of human serum albumin variants. Eight distinguishable types. Hum. Hered., 19 159. | en_US |
dc.identifier.citedreference | Weitkamp, L. R. & Neel, J. V. ( 1972 ). The genetic structure of a tribal population, the Yanomama Indians. IV. Eleven erythrocyte enzymes and summary of protein variants. Ann. Hum. Genet. (Lond.), 35 433. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Renwick, J. H., Berger, J., Shreffler, D. C., Drachmann, O., Wuhrmahn, F., Braend, M. & Franglen, G. ( 1970 ). Additional data and summary for albumin-Ge linkage in man. Hum. Hered., 20 1. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Robson, E. B., Shreffler, D. C. & Corney, G. ( 1968 ). An unusual human scrum albumin variant: Further data on genetic linkage between loci for human serum albumin and group-specific component (Ge). Am. J. Hum. Genet., 20 392. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Rucknagel, D. L. & Gershowitz, H. ( 1966 ). Genetic linkage between structural loci for albumin and group specific component (Ge). Am. J. Hum. Genet., 18 559. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Shreffler, D. C., Robbins, J. L., Drachmann, O., Adner, P. L., Wieme, R. J., Simon, N. M., Cooke, K. B., Sandor, G., Whurmann, F., Braend, M. & TÁrnoky, A. L. ( 1907 ). An electro-phoretic comparison of serum albumin variants from nineteen unrelated families. Acta Genet. Stat. Med., 17 399. | en_US |
dc.identifier.citedreference | Weitkamp, L. R., Shreffler, D. C. & Saave, J. ( 1969 ). Serum albumin variants in New Guinea indigenes. Vox Sang., 17 237. | en_US |
dc.identifier.citedreference | Welch, S. G. ( 1971 ). Qualitative and quantitative variants of human phosphoglucose isomerase. Hum. Hered., 21 467. | en_US |
dc.identifier.citedreference | Wieme, R. J. ( 1900 ). On the presence of two albumins in certain normal human sera arid its genetic determination. Clin. Chim. Acta, 5 443. | en_US |
dc.identifier.citedreference | Winter, W. P., Weitkamp, L. R. & Rucknagel, D. L. ( 1972 ). Amino acid substitution in two identical inherited human serum albumin variants: albumin Oliphant and albumin Ann Arbor. Biochemistry, 11 889. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.