Your browser doesn't support javascript.
loading
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.
Ravindran, Ethiraj; Arashiki, Nobuto; Becker, Lena-Luise; Takizawa, Kohtaro; Lévy, Jonathan; Rambaud, Thomas; Makridis, Konstantin L; Goshima, Yoshio; Li, Na; Vreeburg, Maaike; Demeer, Bénédicte; Dickmanns, Achim; Stegmann, Alexander P A; Hu, Hao; Nakamura, Fumio; Kaindl, Angela M.
Afiliação
  • Ravindran E; Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Arashiki N; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Becker LL; Institute for Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Takizawa K; Department of Biochemistry, Tokyo Women's Medical University, Tokyo, Japan.
  • Lévy J; Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Rambaud T; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Makridis KL; Institute for Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Goshima Y; Department of Biochemistry, Tokyo Women's Medical University, Tokyo, Japan.
  • Li N; Department of Genetics, Robert Debré University Hospital, Paris, France.
  • Vreeburg M; Laboratoire de biologie médicale multisites Seqoia, Paris, France.
  • Demeer B; Laboratoire de biologie médicale multisites Seqoia, Paris, France.
  • Dickmanns A; Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Stegmann APA; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Hu H; Institute for Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Nakamura F; Department of Molecular Pharmacology and Neurobiology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
  • Kaindl AM; Laboratory of Medical Systems Biology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Elife ; 112022 12 13.
Article em En | MEDLINE | ID: mdl-36511780
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Deficiência Intelectual Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Deficiência Intelectual Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha