Your browser doesn't support javascript.
loading
Identification of novel variations in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
Li, Shang; Hu, Hua-Ying; Xu, Jun-Jun; Feng, Zhan-Ke; Sun, Yong-Qing; Chen, Xu; Yang, Kai; Li, Ya-Zhou; Zhang, Dong-Liang.
Afiliação
  • Li S; Department of Anesthesiology, Peking University People's Hospital, Beijing, China.
  • Hu HY; Jiaen Genetics Laboratory, Beijing Jiaen Hospital, Beijing, China.
  • Xu JJ; Department of Anesthesiology, Peking University People's Hospital, Beijing, China.
  • Feng ZK; Jiaen Genetics Laboratory, Beijing Jiaen Hospital, Beijing, China.
  • Sun YQ; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
  • Chen X; Department of Orthodontics, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing, China.
  • Yang K; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
  • Li YZ; Department of Pediatric Orthopedics, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
  • Zhang DL; Department of Orthodontics, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing, China.
Mol Genet Genomic Med ; 9(11): e1839, 2021 11.
Article em En | MEDLINE | ID: mdl-34674383
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatias Hereditárias Sensoriais e Autônomas / Insensibilidade Congênita à Dor / Receptor trkA / Hipo-Hidrose Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatias Hereditárias Sensoriais e Autônomas / Insensibilidade Congênita à Dor / Receptor trkA / Hipo-Hidrose Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article