A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants-Reference-Cited by-同舟云学术

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants

Published:2015-02-04 Issue:10 Volume:23 Page:1318-1327
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Lenassi Eva,Vincent Ajoy^ORCID,Li Zheng,Saihan Zubin,Coffey Alison J,Steele-Stallard Heather B,Moore Anthony T,Steel Karen P,Luxon Linda M,Héon Elise,Bitner-Glindzicz Maria,Webster Andrew R

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2014283.pdf

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