[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

Liu, J X; Wang, C J; Dai, J H; Zhang, M X; Lyu, B; Jiang, Bin.

Afiliação

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 em Zh | MEDLINE | ID: mdl-35090252

Assuntos

Afibrinogenemia; Afibrinogenemia/genética; Idoso; Fibrinogênio/genética; Heterozigoto; Humanos; Masculino; Mutação; Linhagem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Afibrinogenemia Limite: Aged / Humans / Male Idioma: Zh Revista: Zhonghua Nei Ke Za Zhi Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

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