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Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders.
Quan, Yingting; Zhang, Qiumeng; Chen, Meilin; Wu, Huidan; Ou, Jianjun; Shen, Yidong; Li, Kuokuo; Xun, Guanglei; Zhao, Jingping; Hu, Zhengmao; Xia, Kun; Guo, Hui.
Afiliação
  • Quan Y; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Zhang Q; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Chen M; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Wu H; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Ou J; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Shen Y; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Li K; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Xun G; Mental Health Center of Shandong Province, Jinan, Shandong, China.
  • Zhao J; Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Hu Z; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Xia K; Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Guo H; Collaborative Innovation Center for Genetics and Development, Shanghai, China.
J Mol Neurosci ; 70(12): 2085-2092, 2020 Dec.
Article em En | MEDLINE | ID: mdl-32524419
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas Repressoras / Receptores Citoplasmáticos e Nucleares / Transtorno do Espectro Autista Limite: Child / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas Repressoras / Receptores Citoplasmáticos e Nucleares / Transtorno do Espectro Autista Limite: Child / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article