De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement-Reference-Cited by-同舟云学术

De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement

Published:2022-10 Issue:10 Volume:109 Page:1932-1943
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lu Shenzhao,Ma Mengqi,Mao Xiao,Bacino Carlos A.,Jankovic Joseph,Sutton V. Reid,Bartley James A.,Wang Xueying,Rosenfeld Jill A.,Beleza-Meireles Ana,Chauhan Jaynee,Pan Xueyang,Li Megan,Liu Pengfei,Prescott Katrina,Amin Sam,Davies George,Wangler Michael F.,Dai Yuwei,Bellen Hugo J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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