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Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4 : Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

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Title
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4 : Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
Author(s)
Makishima, Tomoko; Madeo, Anne C.; Brewer, Carmen C.; Zalewski, Christopher K.; Butman, John A.; Sachdev, Vandana; Arai, Andrew E.; Holbrook, Brenda M.; Rosing, Douglas R.; Griffith, Andrew J.
Journal
American Journal of Medical Genetics , Volume 143A (14) Wiley – Jul 15, 2007
Publisher
Wiley Subscription Services, Inc., A Wiley Company
Copyright
Copyright © 2007 Wiley‐Liss, Inc., A Wiley Company
ISSN
0148-7299
eISSN
1096-8628
D.O.I.
10.1002/ajmg.a.31793
Publisher site
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