Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice

Author:

Anzai Takashi,Fukunaga Ichiro,Hatakeyama Kaori,Fujimoto Ayumi,Kobayashi Kazuma,Nishikawa Atena,Aoki Toru,Noda Tetsuo,Minowa Osamu,Ikeda Katsuhisa,Kamiya Kazusaku

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference36 articles.

1. Connexin-26-associated deafness: phenotypic variability and progression of hearing loss;DK Chan;Genetics in medicine: official journal of the American College of Medical Genetics,2010

2. Universal infant hearing screening by automated auditory brainstem response measurement;JA Mason;Pediatrics,1998

3. Non-syndromic, autosomal-recessive deafness;MB Petersen;Clinical genetics,2006

4. Genetic epidemiology of hearing impairment;NE Morton;Annals of the New York Academy of Sciences,1991

5. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene;R Birkenhager;American journal of medical genetics Part A,2010

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