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Case Reports
. 2016 Dec;37(4):468-470.
doi: 10.3109/13816810.2015.1120318. Epub 2016 Mar 11.

CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype

Maxwell W Dixon  1 , Maxwell S Stem  2 , Jane L Schuette  3   4 , Catherine E Keegan  3   4 , Cagri G Besirli  2
Affiliations
Case Reports

CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype

Maxwell W Dixon et al. Ophthalmic Genet. 2016 Dec.
No abstract available

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