A genetic approach to understanding inner ear function

Journal of Clinical Investigation

Volumn 106, Issue 12, 2000, Pages 1431-1432

  Battey J F , Jr ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COCHLEA; GENE FUNCTION; HEARING; HEARING IMPAIRMENT; HEREDITY; HUMAN; INNER EAR; NONHUMAN; NOTE; POTASSIUM TRANSPORT; PRIORITY JOURNAL; VESTIBULAR SYSTEM;

EID: 0034521378     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/jci11763     Document Type: Note

References (17)

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7. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
8. Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice
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17. Prestin is the motor protein of cochlear outer hair cells