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RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease.
Wontakal, Sandeep N; Britto, Mishan; Zhang, Huan; Han, Yongshuai; Gao, Chengjie; Tannenbaum, Sarah; Durham, Benjamin H; Lee, Margaret T; An, Xiuli; Mishima, Masanori.
Afiliación
  • Wontakal SN; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY.
  • Britto M; Centre for Mechanochemical Cell Biology & Division of Biomedical Sciences, Warwick Medical School, University of Warwick, Coventry, United Kingdom.
  • Zhang H; Laboratory of Membrane Biology, New York Blood Center, New York, NY.
  • Han Y; Laboratory of Membrane Biology, New York Blood Center, New York, NY.
  • Gao C; Laboratory of Membrane Biology, New York Blood Center, New York, NY.
  • Tannenbaum S; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY; and.
  • Durham BH; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY.
  • Lee MT; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • An X; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY; and.
  • Mishima M; Laboratory of Membrane Biology, New York Blood Center, New York, NY.
Blood ; 139(9): 1413-1418, 2022 03 03.
Article en En | MEDLINE | ID: mdl-34818416
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Activadoras de GTPasa / Anemia Diseritropoyética Congénita Límite: Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Activadoras de GTPasa / Anemia Diseritropoyética Congénita Límite: Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article