A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3

American Journal of Human Genetics

Volumn 65, Issue 1, 1999, Pages 141-150

  Fukushima, Kunihiro ^a   Kasai, Norio ^a   Ueki, Yasuyoshi ^b,c   Nishizaki, Kazunori ^a   Sugata, Kennichi ^a   Hirakawa, Satoshi ^b   Masuda, Akemi ^a   Gunduz, Mehmet ^a   Ninomiya, Yoshifumi ^b   Masuda, Yu ^a   Sato, Minako ^a   McGuirt, Wyman T ^a   Coucke, Paul ^d   Van Camp, Guy ^d   Smith, Richard J H ^a,b  

^a OKAYAMA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b UNIVERSITY OF IOWA HEALTH CARE   (United States)

^c KEIO UNIVERSITY   (Japan)

^d UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROCORTISONE; PREDNISOLONE; SODIUM CHANNEL; STEROID;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHANNEL GATING; CHILD; CHROMOSOME 2Q; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HEARING LOSS; HUMAN; MALE; PHENOTYPE; POSITION EFFECT; PRIORITY JOURNAL; STEROID THERAPY;

EID: 0033362452     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302461     Document Type: Article

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