Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

Published 2014 View Full Article

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Title
Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 94, Issue 2, Pages 295-302
Publisher
Elsevier BV
Online
2014-01-24
DOI
10.1016/j.ajhg.2014.01.001

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