GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Published 2009 View Full Article

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Title
GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
Authors
Keywords
-
Journal
HUMAN MUTATION
Volume 30, Issue 5, Pages 724-733
Publisher
Wiley
Online
2009-04-01
DOI
10.1002/humu.20958

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