Identification of a recurrent missense mutation in the FGA gene likely causing a congenital fibrinogen disorder.

Gao, Runguang; Bi, Meixia; Li, Bei; Yue, Xiaojing; Yuan, Fang; Zhang, Xiaoke; Wang, Xiong

Gao, Runguang; Bi, Meixia; Li, Bei; Yue, Xiaojing; Yuan, Fang; Zhang, Xiaoke; Wang, Xiong.

Afiliación

Gao R; Department of Laboratory Medicine, Jiaozuo Women's and Children's Hospital.
Bi M; Department of Laboratory Medicine, Jiaozuo Hospital of Traditional Chinese Medicine, Jiaozuo.
Li B; Department of Laboratory Medicine, Jiaozuo Women's and Children's Hospital.
Yue X; Department of Laboratory Medicine, Jiaozuo Women's and Children's Hospital.
Yuan F; Department of Laboratory Medicine, Jiaozuo Women's and Children's Hospital.
Zhang X; Department of Laboratory Medicine, Jiaozuo Women's and Children's Hospital.
Wang X; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Blood Coagul Fibrinolysis ; 32(6): 424-426, 2021 09 01.

Article en En | MEDLINE | ID: mdl-34102653

Asunto(s)

Afibrinogenemia/genética; Fibrinógeno/genética; Mutación Missense; Adulto; Anciano; Pueblo Asiatico/genética; Femenino; Humanos; Lactante; Masculino; Persona de Mediana Edad; Linaje; Embarazo

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Mutación Missense / Afibrinogenemia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Infant / Male / Middle aged / Pregnancy Idioma: En Revista: Blood Coagul Fibrinolysis Asunto de la revista: ANGIOLOGIA / HEMATOLOGIA Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido

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