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Ophthalmic Genetics
Volume 37, 2016 - Issue 4
433
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Letters to the Journal
CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype
Maxwell W. Dixon University of Michigan Medical School, Ann Arbor, Michigan, USA
, Maxwell S. Stem W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan, USA
, Jane L. Schuette Department of Pediatrics, Division of Genetics, University of Michigan, Ann Arbor, Michigan, USA; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA
, Catherine E. Keegan Department of Pediatrics, Division of Genetics, University of Michigan, Ann Arbor, Michigan, USA; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA
& Cagri G. Besirli W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan, USACorrespondencecbesirli@med.umich.edu
Pages 468-470
Published online: 11 Mar 2016
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