Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F-Reference-Cited by-同舟云学术

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Published:2001-07 Issue:1 Volume:69 Page:25-34
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ahmed Zubair M.,Riazuddin Saima,Bernstein Steve L.,Ahmed Zahoor,Khan Shaheen,Griffith Andrew J.,Morell Robert J.,Friedman Thomas B.,Riazuddin Sheikh,Wilcox Edward R.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference52 articles.

1. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nat Genet,2001

2. The cadherin superfamily: diversity in form and function;Angst;J Cell Sci,2001

3. Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I;Astuto;Am J Hum Genet,2000

4. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene;Bitner-Glindzicz;Nat Genet,2000

5. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D;Bolz;Nat Genet,2001

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