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Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders.
Pang, Nan; Li, Kuokuo; Tan, Senwei; Chen, Meilin; He, Fang; Chen, Chen; Yang, Lifen; Zhang, Ciliu; Deng, Xiaolu; Yang, Li; Mao, Leilei; Wang, Guoli; Duan, Haolin; Wang, Xiaole; Zhang, Wen; Guo, Hui; Peng, Jing; Yin, Fei; Xia, Kun.
Affiliation
  • Pang N; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Li K; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
  • Tan S; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
  • Chen M; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
  • He F; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Chen C; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Yang L; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Zhang C; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Deng X; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Yang L; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Mao L; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Wang G; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Duan H; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Wang X; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Zhang W; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Guo H; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
  • Peng J; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China. Electronic address: pengjing4346@163.com.
  • Yin F; Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China. Electronic address: yf2323@hotmail.com.
  • Xia K; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; Hengyang Medical School, 421001, University of South, China. Electronic address: xiakun@sklmg.edu.cn.
Gene ; 897: 148071, 2024 Mar 01.
Article in En | MEDLINE | ID: mdl-38081334
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Neurodevelopmental Disorders / Autism Spectrum Disorder / Intellectual Disability Limits: Humans Language: En Journal: Gene Year: 2024 Document type: Article Affiliation country:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Neurodevelopmental Disorders / Autism Spectrum Disorder / Intellectual Disability Limits: Humans Language: En Journal: Gene Year: 2024 Document type: Article Affiliation country: