Nonsyndromic hearing loss DFNA10 and a novel mutation ofEYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain-Reference-Cited by-同舟云学术

Nonsyndromic hearing loss DFNA10 and a novel mutation ofEYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

Published:2007-07-15 Issue:14 Volume:143A Page:1592-1598
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

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.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference14 articles.

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2. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23;Bork;Am J Hum Genet,2001

3. The DFNA10 phenotype;De Leenheer;Ann Otol Rhinol Laryngol,2001

4. Human nonsyndromic sensorineural deafness;Friedman;Annu Rev Genomics Hum Genet,2003

5. Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6);Mohiddin;J Med Genet,2004

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