Cochlear histopathology in human genetic hearing loss: State of the science and future prospects-Reference-Cited by-同舟云学术

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Cochlear histopathology in human genetic hearing loss: State of the science and future prospects

Published:2019-10 Issue: Volume:382 Page:107785
ISSN:0378-5955
Container-title:Hearing Research
language:en
Short-container-title:Hearing Research

Author:

Bommakanti Krishna,Iyer Janani S.,Stankovic Konstantina M.

Funder

Lauer Tinnitus Research Center, Massachusetts Eye and Ear

U.S. Department of Defense

Office of Extramural Research, National Institutes of Health

Publisher

Elsevier BV

Subject

Sensory Systems

Reference114 articles.

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

2. Neurofibromatosis type 2;Asthagiri;Lancet (London, England),2009

3. Mouse models for deafness: lessons for the human inner ear and hearing loss;Avraham;Ear Hear.,2003

4. Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion, and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorder;Bae;Hum. Mutat.,2014

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