A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss

Published 2008 View Full Article

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Title
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 16, Issue 5, Pages 593-602
Publisher
Springer Nature
Online
2008-01-23
DOI
10.1038/sj.ejhg.5202000

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