Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation

Ye, Longying; Liu, Meina; Yang, Lihong; Wang, Mingshan; Xie, Yaosheng

Ye, Longying; Liu, Meina; Yang, Lihong; Wang, Mingshan; Xie, Yaosheng.

Afiliación

Ye L; The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China
Liu M; The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China
Yang L; The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China
Wang M; The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China
Xie Y; The First Affiliated Hospital of Wenzhou Medical University, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, Department of Clinical Laboratory, Wenzhou, China

Turk J Haematol ; 41(1): 66-68, 2024 03 01.

Article en En | MEDLINE | ID: mdl-38298123

Asunto(s)

Factor XII; Mutación Missense; Humanos; Mutación; Factor XII/genética

Palabras clave

Factor XII deficiency; Genetic mutation; Novel mutation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor XII / Mutación Missense Límite: Humans Idioma: En Revista: Turk J Haematol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Turquía

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