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.

Affiliation

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 in En | MEDLINE | ID: mdl-38298123

Subject(s)

Factor XII; Mutation, Missense; Humans; Mutation; Factor XII/genetics

Key words

Factor XII deficiency; Genetic mutation; Novel mutation

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor XII / Mutation, Missense Limits: Humans Language: En Journal: Turk J Haematol Year: 2024 Document type: Article Affiliation country: China Country of publication: Turkey

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