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A novel heterozygous SIX1 missense mutation resulted in non-syndromic unilateral hearing loss.
Li, Ang; Liu, Siwen; Zhang, Peng; Hu, Xintong; Li, Guiying; Gu, Weiyue; Jiang, Yanfang.
Afiliação
  • Li A; Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, Genetic Diagnosis Center, The First Hospital of Jilin University, Changchun, China.
  • Liu S; Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, Genetic Diagnosis Center, The First Hospital of Jilin University, Changchun, China.
  • Zhang P; Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, Genetic Diagnosis Center, The First Hospital of Jilin University, Changchun, China.
  • Hu X; Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, Genetic Diagnosis Center, The First Hospital of Jilin University, Changchun, China.
  • Li G; Chigene (Beijing) Translational Medical Research Center Co., Ltd, Beijing, China.
  • Gu W; Chigene (Beijing) Translational Medical Research Center Co., Ltd, Beijing, China.
  • Jiang Y; Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, Genetic Diagnosis Center, The First Hospital of Jilin University, Changchun, China.
Front Genet ; 13: 1047230, 2022.
Article em En | MEDLINE | ID: mdl-36482904
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article