What is the ocular phenotype associated with a single exon 78 deletion in Duchenne muscular dystrophy?

被引：0
|
作者：
Tuy Nga Brignol
Dominique Mornet
Cecilia Montañez
Dora Fix Ventura
Cyrille Vaillend
Alvaro Rendón
机构：
[1] The French Muscular Dystrophy,Medical Affairs Department
[2] Association (AFM-Telethon),PhyMedExp
[3] Université de Montpellier,Departamento de Genética y Biología Molecular
[4] INSERM,Department of Experimental Psychology, Institute of Psychology
[5] CNRS,Paris
[6] Centro de Investigación y de Estudios Avanzados del IPN,Saclay Institute of Neuroscience, UMR 9197, Université Paris Sud, CNRS
[7] Ciudad de,Sorbonne Université
[8] Universidade de São Paulo,undefined
[9] Université Paris Saclay,undefined
[10] INSERM,undefined
[11] CNRS,undefined
[12] Institut de la Vision,undefined
来源：
Journal of Human Genetics | 2020年 / 65卷
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摘要：
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页码：715 / 716
页数：1
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