Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

Published 2013 View Full Article

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Title
Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 93, Issue 1, Pages 67-77
Publisher
Elsevier BV
Online
2013-06-14
DOI
10.1016/j.ajhg.2013.05.015

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