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Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases.
Luo, Xiaomei; Zou, Yongyi; Tan, Bo; Zhang, Yue; Guo, Jing; Zeng, Lanlan; Zhang, Rui; Tan, Hu; Wei, Xianda; Hu, Yiqiao; Zheng, Yu; Liang, Desheng; Wu, Lingqian.
Afiliação
  • Luo X; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Zou Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Tan B; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Zhang Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Guo J; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Zeng L; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Zhang R; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Tan H; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Wei X; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Hu Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Zheng Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Liang D; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Wu L; Hunan Jiahui Genetics Hospital, Changsha, China.
J Hum Genet ; 62(4): 513-516, 2017 Apr.
Article em En | MEDLINE | ID: mdl-28077840
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição GATA / Estudos de Associação Genética / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição GATA / Estudos de Associação Genética / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China