Mouse Models for Deafness: Lessons for the Human Inner Ear and Hearing Loss
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Speech and Hearing,Otorhinolaryngology
Reference73 articles.
1. USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses;Adato;European Journal of Human Genetics,2002
2. Mutations ofMYO6are associated with recessive deafness, DFNB37;Ahmed;American Journal of Human Genetics,2003
3. The mouse Ames waltzer hearing-loss mutant is caused by mutation ofPcdh15, a novel protocadherin gene;Alagramam;Nature Genetics,2001
4. A compendium of mouse knockouts with inner ear defects;Anagnostopoulos;Trends in Genetics,2002
5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;Nature Genetics,1995
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