CTNNB1 mutation associated with familial...

Ophthalmic Genetics 2016 / 03

CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype

Dixon, Maxwell W., Stem, Maxwell S., Schuette, Jane L., Keegan, Catherine E., Besirli, Cagri G.
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Language:
english
Journal:
Ophthalmic Genetics
DOI:
10.3109/13816810.2015.1120318
Date:
March, 2016
File:
PDF, 698 KB
english, 2016
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