PDZD7and hearing loss: More than just a modifier-Reference-Cited by-同舟云学术

PDZD7and hearing loss: More than just a modifier

Published:2015-09-29 Issue:12 Volume:167 Page:2957-2965
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Booth Kevin T.¹,Azaiez Hela¹,Kahrizi Kimia²,Simpson Allen C.¹,Tollefson William T.A.³,Sloan Christina M.¹,Meyer Nicole C.¹,Babanejad Mojgan²,Ardalani Fariba²,Arzhangi Sanaz²,Schnieders Michael J.³,Najmabadi Hossein²,Smith Richard J.H.¹

Affiliation:

1. Department of Otolaryngology-Head Neck Surgery; Molecular Otolaryngology Renal Research Laboratories; University of Iowa; Iowa City Iowa

2. Genetics Research Center; University of Social Welfare and Rehabilitation Sciences; Tehran Iran

3. Department of Biomedical Engineering; University of Iowa; Iowa City Iowa

Funder

National Institute on Deafness and Other Communication Disorders

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37274/fullpdf

Reference35 articles.

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3. Rescue from hearing loss in Usher's syndrome;Avraham;N Engl J Med,2013

4. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss;Azaiez;Hum Mutat,2014

5. R2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice;Azaiez;PLoS Genet,2015

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