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Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.
Zhao, Wenjing; Tan, Jieqiong; Zhu, Tengfei; Ou, Jianjun; Li, Ying; Shen, Lu; Wu, Huidan; Han, Lin; Liu, Yanling; Jia, Xiangbin; Bai, Ting; Li, Honghui; Ke, Xiaoyan; Zhao, Jingping; Zou, Xiaobing; Hu, Zhengmao; Guo, Hui; Xia, Kun.
Afiliação
  • Zhao W; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Tan J; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Zhu T; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Ou J; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, 410011, China.
  • Li Y; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Shen L; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Wu H; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Han L; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Liu Y; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Jia X; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Bai T; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Li H; Key Laboratory of Developmental Disorders in Children, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, 545001, China.
  • Ke X; Child Mental Health Research Center, Nanjing Brain Hospital Affiliated of Nanjing Medical University, Nanjing, 210029, China.
  • Zhao J; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, 410011, China.
  • Zou X; Children Development Behavior Center of the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
  • Hu Z; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China.
  • Guo H; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, 410011, China. Electronic address: guohui@sklmg.edu.cn.
  • Xia K; Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China; School of Life Sciences and Technology, Xinjiang University, Ürümqi, 830046, China; CAS Center for Excellence in Brain Science and Intelligence Techn
J Genet Genomics ; 46(5): 247-257, 2019 05 20.
Article em En | MEDLINE | ID: mdl-31196716
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transposases / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Transtorno do Espectro Autista / Neurônios Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transposases / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Transtorno do Espectro Autista / Neurônios Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article