Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1 , a Gene Implicated in Ubiquitination-Reference-Cited by-同舟云学术

Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1 , a Gene Implicated in Ubiquitination

Published:2016-08 Issue:2 Volume:99 Page:470-480
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Coppieters Frauke,Ascari Giulia,Dannhausen Katharina,Nikopoulos Konstantinos,Peelman Frank,Karlstetter Marcus,Xu Mingchu,Brachet Cécile,Meunier Isabelle,Tsilimbaris Miltiadis K.,Tsika Chrysanthi,Blazaki Styliani V.,Vergult Sarah,Farinelli Pietro,Van Laethem Thalia,Bauwens Miriam,De Bruyne Marieke,Chen Rui,Langmann Thomas,Sui Ruifang,Meire Françoise,Rivolta Carlo,Hamel Christian P.,Leroy Bart P.,De Baere Elfride

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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