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Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang, Yan-Bao; Tang, Shao-Hua; Li, Huan-Zheng; Xu, Chen-Yang; Chen, Chong; Xu, Yun-Zhi; Ding, Li-Rong; Xu, Xue-Qin.
Afiliação
  • Xiang YB; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: bxiangyanbao@163.com.
  • Tang SH; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China; Key Laboratory of Medical Genetic, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China. Electronic address: tsh006@126.com.
  • Li HZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: 13676720736@126.com.
  • Xu CY; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: xcyang@163.com.
  • Chen C; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: chenchong325@foxmail.com.
  • Xu YZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: 15216615932@163.com.
  • Ding LR; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China; Key Laboratory of Medical Genetic, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China. Electronic address: lirongding2016@163.com.
  • Xu XQ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China. Electronic address: xuxueqin0577@126.com.
Int J Pediatr Otorhinolaryngol ; 122: 185-190, 2019 Jul.
Article em En | MEDLINE | ID: mdl-31035178
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico / Conexinas / Surdez / Transportadores de Sulfato Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico / Conexinas / Surdez / Transportadores de Sulfato Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article