Clinical, molecular genetic, and functional analysis of a pedigree with a novel dominant optic atrophy mutation

被引：0
|
作者：
Fingert, John H. [1 ]
van der Heide, Carly [1 ]
Cooke, Jessica A. [1 ]
Roos, Ben R. [1 ]
Jain, Ankur [1 ]
Rodine, Kathy [1 ]
Mullins, Robert F. [1 ]
Tucker, Budd [1 ]
机构：
[1] Univ Iowa, Carver Coll Med, Ophthalmol & Visual Sci, Iowa City, IA USA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2019年 / 60卷 / 09期
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D O I：
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中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
2960
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页数：3
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