MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform-Reference-Cited by-同舟云学术

MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform

Published:2016-02-16 Issue:5 Volume:37 Page:481-487
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Grati M'hamed¹,Yan Denise¹,Raval Manmeet H.²,Walsh Tom³,Ma Qi¹,Chakchouk Imen¹⁴,Kannan-Sundhari Abhiraami¹,Mittal Rahul¹,Masmoudi Saber⁴,Blanton Susan H.¹⁵,Tekin Mustafa¹⁵,King Mary-Claire³,Yengo Christopher M.²,Liu Xue Zhong¹⁵⁶

Affiliation:

1. Department of Otolaryngology; University of Miami Miller School of Medicine; Miami Florida

2. Department of Cellular and Molecular Physiology; Pennsylvania State University College of Medicine; Hershey Pennsylvania

3. Departments of Medicine and Genome Sciences; University of Washington; Seattle Washington

4. Laboratoire Procédés de Criblage Moléculaire et Cellulaire, Centre de Biotechnologie de Sfax; Université de Sfax; Sfax Tunisie

5. Dr. John T. Macdonald Foundation; Department of Human Genetics, and John P. Hussman Institute for Human Genomics; University of Miami; Miami Florida

6. Department of Otolaryngology; Xiangya Hospital; Central South University; Changsha Hunan China

Funder

National Institutes of Health

The American Hearing Research Foundation grant

Pennsylvania Lions Hearing Research Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Genomic advances for gene discovery in hereditary hearing loss;Avraham;J Basic Clin Physiol Pharmacol,2012

2. Kinetic mechanism of human myosin IIIA;Dosé;J Biol Chem,2007