Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration-Reference-Cited by-同舟云学术

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

Published:2012-07-29 Issue:9 Volume:44 Page:1035-1039
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Koenekoop Robert K, ,Wang Hui,Majewski Jacek,Wang Xia,Lopez Irma,Ren Huanan,Chen Yiyun,Li Yumei,Fishman Gerald A,Genead Mohammed,Schwartzentruber Jeremy,Solanki Naimesh,Traboulsi Elias I,Cheng Jingliang,Logan Clare V,McKibbin Martin,Hayward Bruce E,Parry David A,Johnson Colin A,Nageeb Mohammed,Poulter James A,Mohamed Moin D,Jafri Hussain,Rashid Yasmin,Taylor Graham R,Keser Vafa,Mardon Graeme,Xu Huidan,Inglehearn Chris F,Fu Qing,Toomes Carmel,Chen Rui

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2356.pdf

Reference29 articles.

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