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Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
Xiang, Yan-Bao; Xu, Chen-Yang; Xu, Yun-Zhi; Li, Huan-Zheng; Zhou, Li-Li; Xu, Xue-Qin; Chen, Zi-Hui; Tang, Shao-Hua.
Afiliación
  • Xiang YB; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu CY; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu YZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Li HZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Zhou LL; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu XQ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Chen ZH; Key laboratory of Medical Genetic, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China.
  • Tang SH; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
Mol Genet Genomic Med ; 8(12): e1539, 2020 12.
Article en En | MEDLINE | ID: mdl-33095980
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sordera / Sitios Genéticos / Mutación Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sordera / Sitios Genéticos / Mutación Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos