WDR19 : An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome
dc.contributor.author | Coussa, R G | en_US |
dc.contributor.author | Otto, E A | en_US |
dc.contributor.author | Gee, H‐y | en_US |
dc.contributor.author | Arthurs, P | en_US |
dc.contributor.author | Ren, H | en_US |
dc.contributor.author | Lopez, I | en_US |
dc.contributor.author | Keser, V | en_US |
dc.contributor.author | Fu, Q | en_US |
dc.contributor.author | Faingold, R | en_US |
dc.contributor.author | Khan, A | en_US |
dc.contributor.author | Schwartzentruber, J | en_US |
dc.contributor.author | Majewski, J | en_US |
dc.contributor.author | Hildebrandt, F | en_US |
dc.contributor.author | Koenekoop, R K | en_US |
dc.date.accessioned | 2013-08-02T20:51:23Z | |
dc.date.available | 2014-10-06T19:17:44Z | en_US |
dc.date.issued | 2013-08 | en_US |
dc.identifier.citation | Coussa, R G; Otto, E A; Gee, H‐y ; Arthurs, P; Ren, H; Lopez, I; Keser, V; Fu, Q; Faingold, R; Khan, A; Schwartzentruber, J; Majewski, J; Hildebrandt, F; Koenekoop, R K (2013). " WDR19 : An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Seniorâ Loken syndrome." Clinical Genetics 84(2): 150-159. <http://hdl.handle.net/2027.42/99013> | en_US |
dc.identifier.issn | 0009-9163 | en_US |
dc.identifier.issn | 1399-0004 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/99013 | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.publisher | Wiley Periodicals, Inc. | en_US |
dc.subject.other | Retinitis Pigmentosa | en_US |
dc.subject.other | Senior‐LøKen Syndrome | en_US |
dc.subject.other | WDR19 | en_US |
dc.subject.other | Childhood Blindness | en_US |
dc.subject.other | IFT144 | en_US |
dc.subject.other | IFT ‐A | en_US |
dc.subject.other | Nephronophtisis | en_US |
dc.subject.other | Photoreceptors | en_US |
dc.subject.other | Retinal Degeneration | en_US |
dc.title | WDR19 : An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome | 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.affiliationother | Department of Radiology | en_US |
dc.contributor.affiliationother | Department of Ophthalmology | en_US |
dc.contributor.affiliationother | Department of Paediatric Surgery | en_US |
dc.identifier.pmid | 23683095 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/99013/1/cge12196.pdf | |
dc.identifier.doi | 10.1111/cge.12196 | en_US |
dc.identifier.source | Clinical Genetics | en_US |
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dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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