Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators

Title
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators
Authors
Keywords
-
Journal
HUMAN GENETICS
Volume 126, Issue 6, Pages 791-803
Publisher
Springer Nature
Online
2009-08-13
DOI
10.1007/s00439-009-0730-x

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