[The clinical phenotype and gene analysis of syndromic deafness with <i>PTPN11</i> gene mutation].

Gao, Y; Li, Z C; Ma, X L; Gao, Y Q; Xiao, Y; Dai, X; Ma, J

[The clinical phenotype and gene analysis of syndromic deafness with PTPN11 gene mutation].

Gao, Y; Li, Z C; Ma, X L; Gao, Y Q; Xiao, Y; Dai, X; Ma, J.

Afiliação

Gao Y; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Li ZC; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Ma XL; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Gao YQ; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Xiao Y; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Dai X; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China.
Ma J; Department of Otorhinolaryngology Head and Neck Surgery, Kunming Children's Hospital, Kunming 650228, China Kunming Key Laboratory for Prevention and Control of Congenital Birth Defects of Children, Kunming 650228, China.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi ; 57(3): 317-323, 2022 Mar 07.

Article em Zh | MEDLINE | ID: mdl-35325944

Assuntos

Surdez; Perda Auditiva; Surdez/genética; Testes Genéticos; Perda Auditiva/genética; Humanos; Masculino; Mutação; Fenótipo; Proteína Tirosina Fosfatase não Receptora Tipo 11/genética

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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Surdez / Perda Auditiva Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: Zh Revista: Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

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