Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

Published 2008 View Full Article

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Title
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 83, Issue 1, Pages 18-29
Publisher
Elsevier BV
Online
2008-06-06
DOI
10.1016/j.ajhg.2008.05.012

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