Strain background effects and genetic modifiers of hearing in mice
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience
Reference73 articles.
1. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation;Abe;Am. J. Med. Genet.,2001
2. Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance;Adato;Am. J. Hum. Genet.,1999
3. USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses;Adato;Eur. J. Hum. Genet.,2002
4. Mouse models for human deafness: current tools for new fashions;Ahituv;Trends Mol. Med.,2002
5. Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family;Balciuniene;Am. J. Hum. Genet.,1998
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