Genetics of Hearing and Deafness-Reference-Cited by-同舟云学术

Genetics of Hearing and Deafness

Published:2012-10-08 Issue:11 Volume:295 Page:1812-1829
ISSN:1932-8486
Container-title:The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology
language:en
Short-container-title:Anat Rec

Author:

Angeli Simon,Lin Xi,Liu Xue Zhong

Publisher

Wiley

Subject

Ecology, Evolution, Behavior and Systematics,Histology,Biotechnology,Anatomy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ar.22579/fullpdf

Reference126 articles.

1. Interactions in the network of Usher syndrome type 1 proteins;Adato;Hum Mol Genet,2005

2. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness;Ahmad;Proc Natl Acad Sci USA,2007

3. A new mouse insertional mutation that causes sensorineural deafness and vestibular defects;Alagramam;Genetics,1999

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

5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;NatGenet,1995

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