Homozygosity for a novel truncating mutation confirmsTBX15deficiency as the cause of Cousin syndrome

Title
Homozygosity for a novel truncating mutation confirmsTBX15deficiency as the cause of Cousin syndrome
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 161, Issue 12, Pages 3161-3165
Publisher
Wiley
Online
2013-08-17
DOI
10.1002/ajmg.a.36173

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