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Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencing.
Miyagawa, Maiko; Nishio, Shin-Ya; Ichinose, Aya; Iwasaki, Satoshi; Murata, Takaaki; Kitajiri, Shin-Ichiro; Usami, Shin-Ichi.
Afiliação
  • Miyagawa M; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto, Japan.
  • Nishio SY; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ichinose A; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan.
  • Iwasaki S; Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto, Japan Department of Otorhinolaryngology, International University of Health and Welfare, Mita Hospital, Tokyo, Japan.
  • Murata T; Department of Otorhinolaryngology, Gunma University School of Medicine, Maebashi, Japan.
  • Kitajiri S; Department of Otorhinolaryngology-Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Usami S; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto, Japan usami@shinshu-u.ac.jp.
Ann Otol Rhinol Laryngol ; 124 Suppl 1: 84S-93S, 2015 May.
Article em En | MEDLINE | ID: mdl-25792668

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Actinas / Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Perda Auditiva / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Actinas / Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Perda Auditiva / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article