Recent Advances in the Understanding of Syndromic Forms of Hearing Loss-Reference-Cited by-同舟云学术

Recent Advances in the Understanding of Syndromic Forms of Hearing Loss

Published:2003-08 Issue:4 Volume:24 Page:289-302
ISSN:0196-0202
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Friedman Thomas B.,Schultz Julie M.,Ben-Yosef Tamar,Pryor Shannon P.,Lagziel Ayala,Fisher Rachel A.,Wilcox Edward R.,Riazuddin Saima,Ahmed Zubair M.,Belyantseva Inna A.,Griffith Andrew J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference61 articles.

1. USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses;Adato;European Journal of Human Genetics,2002

2. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F;Ahmed;The American Journal of Human Genetics,2001

3. The medical genetics of Usher syndrome;Ahmed;Clinical Genetics,2003

4. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC;Ahmed;Human Genetics,2002

5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nature Genetics,2001

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