Art

J-GLOBAL ID：200902151541456996   Reference number：98A0671769

Genetic and Clinical Features of Sensorineural Hearing Loss Associated with the 1555 Mitochondrial Mutation.

ミトコンドリアDNA1555変異による難聴

Author (2)： SHINKAWA HIDEICHI (弘前大 医) ,  USAMI SHIN'ICHI (弘前大 医)
Material： 耳鼻咽喉科臨床  (Plactica Oto-Rhino-Laryngologica (Kyoto))
Volume： 91  Issue： 7  Page： 661-668  Publication year： Jul. 1998 
JST Material Number： G0710A  ISSN： 0032-6313  CODEN： JIBIA  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： *mitochondrial gene ,...
Semi thesaurus term： idiopathic disease

   To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=98A0671769&from=J-GLOBAL&jstjournalNo=G0710A") }}

JST classification (2)： Diseases of ear,nose,pharynx and larynx  (GQ03000X) ,  Molecular genetics in general  (EC02010J)

Reference (23)：

• PRAZIC, M. Familial sensitivity to streptomycin. J Laryngol Otol. 1964, 78, 1037-1043
• TSUIKI, T. Familial incidence of streptomycin hearing loss and hereditary weakness of the cochlea. Audiology. 1971, 10, 315-322
• JOHNSONBAUGH, RE. Familial occurrence of drug-induced hearing loss. Am J Dis Child. 1974, 127, 245-247
• DONALD, RR. Streptomycin ototoxicity in the unborn child. South Med J. 1981, 66, 316-318
• VIJOEN, DL. Familial aggregation of streptomycin ototoxicity; autosomal dominant inheritance. J Med Genet. 1983, 20, 357-360

Terms in the title (2)： 変異 ,  難聴