Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice

Genomics

Volumn 74, Issue 2, 2001, Pages 228-233

  Wilson, Scott M ^a   Householder, Deborah B ^a   Coppola, Vincenzo ^a   Tessarollo, Lino ^a   Fritzsch, Bernd ^b   Lee, E Chiang ^a   Goss, Dee ^c   Carlson, George A ^c   Copeland, Neal G ^a   Jenkins, Nancy A ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c MCLAUGHLIN RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; DNA; PROTEIN CDH 23; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; GENE EXPRESSION; GENE INSERTION; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HEARING LOSS; HUMAN; IN SITU HYBRIDIZATION; INNER EAR; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STEREOCILIUM; VESTIBULAR DISORDER;

EID: 0035366320     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2001.6554     Document Type: Article

References (35)

1. The mouse ames waltzer hearing-loss mutant is caused by mutation of pcdh15, a novel protocadherin gene
2. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
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