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[Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
Liu, J X; Wang, C J; Dai, J H; Zhang, M X; Lyu, B; Jiang, Bin.
Afiliación
  • Liu JX; Department of Hematology, Peking University International Hospital, Beijing 102206, China.
  • Wang CJ; Department of Hematology, Peking University International Hospital, Beijing 102206, China.
  • Dai JH; Department of Clinical Laboratory, Peking University International Hospital, Beijing 102206, China.
  • Zhang MX; Department of Hematology, Peking University International Hospital, Beijing 102206, China.
  • Lyu B; Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing 100044, China.
  • Jiang B; Department of Hematology, Peking University International Hospital, Beijing 102206, China.
Zhonghua Nei Ke Za Zhi ; 61(2): 172-176, 2022 Feb 01.
Article en Zh | MEDLINE | ID: mdl-35090252
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Afibrinogenemia Límite: Aged / Humans / Male Idioma: Zh Revista: Zhonghua Nei Ke Za Zhi Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Afibrinogenemia Límite: Aged / Humans / Male Idioma: Zh Revista: Zhonghua Nei Ke Za Zhi Año: 2022 Tipo del documento: Article País de afiliación: China