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Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.
Geng, Xingzhu; Liu, Yanshan; Ren, XiuZhi; Guan, Yun; Wang, Yanzhou; Mao, Bin; Zhao, Xiuli; Zhang, Xue.
Affiliation
  • Geng X; 1 McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, China.
  • Liu Y; 1 McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, China.
  • Ren X; 2 The People's Hospital of Wuqing District, Tianjin, China.
  • Guan Y; 3 Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, School of Medicine, Baltimore, USA.
  • Wang Y; 4 Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
  • Mao B; 1 McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, China.
  • Zhao X; 1 McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, China.
  • Zhang X; 1 McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, China.
Mol Pain ; 14: 1744806918781140, 2018.
Article in En | MEDLINE | ID: mdl-29770739
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Sensory and Autonomic Neuropathies / Receptor, trkA / Asian People / Mutation Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Mol Pain Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA / PSICOFISIOLOGIA Year: 2018 Document type: Article Affiliation country: China Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hereditary Sensory and Autonomic Neuropathies / Receptor, trkA / Asian People / Mutation Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Mol Pain Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA / PSICOFISIOLOGIA Year: 2018 Document type: Article Affiliation country: China Country of publication: United States