Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment-Reference-Cited by-同舟云学术

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment

Published:2013-04-11 Issue:15 Volume:22 Page:3174-3185
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Kirin Mirna,Chandra Aman,Charteris David G.,Hayward Caroline,Campbell Susan,Celap Ivana,Bencic Goran,Vatavuk Zoran,Kirac Iva,Richards Allan J.,Tenesa Albert,Snead Martin P.,Fleck Brian W.,Singh Jaswinder,Harsum Steven,MacLaren Robert E.,den Hollander Anneke I.,Dunlop Malcolm G.,Hoyng Carel B.,Wright Alan F.,Campbell Harry,Vitart Veronique,Mitry Danny

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/22/15/3174/17260216/ddt169.pdf

Reference56 articles.

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2. Pigment epithelial cell ensheathment of cone outer segments in the retina of the domestic cat;Steinberg;Proc. R. Soc. Lond. B Biol. Sci.,1974

3. Racial difference in the incidence of retinal detachment in Singapore;Wong;Arch. Ophthalmol.,1999

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