Molecular diagnosis of deafness: Impact of gene identification

Audiology and Neuro-Otology

Volumn 7, Issue 3, 2002, Pages 185-190

  Usami, Shin Ichi ^a   Koda, Eiko ^a   Tsukamoto, Koji ^a   Otsuka, Akihiro ^a   Yuge, Isamu ^a   Asamura, Kenji ^a   Abe, Satoko ^b   Akita, Jiro ^b   Namba, Atsushi ^b  

^a SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b HIROSAKI UNIVERSITY   (Japan)

Author keywords

Deafness; Gene; GJB2(connexin 26); Mitochondria; PDS

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT;

CONFERENCE PAPER; DIAGNOSTIC APPROACH ROUTE; DISEASE ASSOCIATION; GENE IDENTIFICATION; GENE MUTATION; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; MITOCHONDRION; MUTATION RATE; NONHUMAN; OUTPATIENT; PENDRED SYNDROME; PRIORITY JOURNAL; PROPHYLAXIS; VESTIBULE AQUEDUCT;

CARRIER PROTEINS; CONNEXINS; DEAFNESS; ENDOLYMPHATIC SAC; GENE EXPRESSION; HUMANS; MAGNETIC RESONANCE IMAGING; MEMBRANE TRANSPORT PROTEINS; MOLECULAR BIOLOGY; POINT MUTATION; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0036281380     PISSN: 14203030     EISSN: None     Source Type: Journal    
DOI: 10.1159/000058308     Document Type: Conference Paper

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