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Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population.
Taniguchi, Mirei; Matsuo, Hirotaka; Shimizu, Seiko; Nakayama, Akiyoshi; Suzuki, Koji; Hamajima, Nobuyuki; Shinomiya, Nariyoshi; Nishio, Shinya; Kosugi, Shinji; Usami, Shin-Ichi; Ito, Juichi; Kitajiri, Shin-ichiro.
Afiliación
  • Taniguchi M; Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Matsuo H; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan.
  • Shimizu S; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan.
  • Nakayama A; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan.
  • Suzuki K; Department of Public Health, Fujita Health University School of Medicine, Toyoake, Japan.
  • Hamajima N; Department of Healthcare Administration, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Shinomiya N; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan.
  • Nishio S; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kosugi S; Department of Medical Ethics/Medical Genetics, Kyoto University School of Public Health, Kyoto, Japan.
  • Usami S; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ito J; Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Kitajiri S; Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
J Hum Genet ; 60(10): 613-7, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26178431
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Conexinas / Pueblo Asiatico / Frecuencia de los Genes / Pérdida Auditiva Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Conexinas / Pueblo Asiatico / Frecuencia de los Genes / Pérdida Auditiva Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido