CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype.
作者信息
Dixon Maxwell W, Stem Maxwell S, Schuette Jane L, Keegan Catherine E, Besirli Cagri G
机构信息
a University of Michigan Medical School , Ann Arbor , Michigan , USA.
b W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences , University of Michigan , Ann Arbor , Michigan , USA.
出版信息
Ophthalmic Genet. 2016 Dec;37(4):468-470. doi: 10.3109/13816810.2015.1120318. Epub 2016 Mar 11.
Abstract
摘要
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