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Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.
Yuan, Dejian; Yan, Tizhen; Luo, Shiqiang; Huang, Jun; Tan, Jianqiang; Zhang, Jianping; Zhang, Victor Wei; Lan, Yueyuan; Hu, Taobo; Guo, Jing; Huang, Mingwei; Zeng, Dingyuan.
Afiliación
  • Yuan D; Department of Medical Genetics, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Yan T; Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Luo S; Department of Medical Genetics, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Huang J; Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Tan J; Department of Medical Genetics, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Zhang J; Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Zhang VW; Department of Medical Genetics, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Lan Y; Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Hu T; Department of Medical Genetics, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Guo J; Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Huang M; Department of Ophthalmology, Liuzhou Municipal Maternity and Child Healthcare Hospital, Liuzhou, China.
  • Zeng D; AmCare Genomics Laboratory, Guangzhou, China.
Front Genet ; 12: 765503, 2021.
Article en En | MEDLINE | ID: mdl-34966409

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza