Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

Published 2010 View Full Article

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Title
Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 86, Issue 6, Pages 949-956
Publisher
Elsevier BV
Online
2010-05-21
DOI
10.1016/j.ajhg.2010.04.012

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