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Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.
Cai, Xin Zhang; Li, Ying; Xia, Lu; Peng, Yu; He, Chu Feng; Jiang, Lu; Feng, Yong; Xia, Kun; Liu, Xue Zhong; Mei, Ling Yun; Hu, Zheng Mao.
Afiliación
  • Cai XZ; Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
  • Li Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Xia L; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Peng Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • He CF; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Jiang L; Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
  • Feng Y; Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
  • Xia K; Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, China.
  • Liu XZ; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Mei LY; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Hu ZM; School of Biological Science and Technology, Central South University, Changsha, China.
J Hum Genet ; 62(2): 317-320, 2017 Feb.
Article en En | MEDLINE | ID: mdl-27535032
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Proteínas de Homeodominio / Factor de Transcripción Brn-3C / Pérdida Auditiva Sensorineural Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Proteínas de Homeodominio / Factor de Transcripción Brn-3C / Pérdida Auditiva Sensorineural Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido