Compound heterozygosity for novel von Willebrand factor genetic variants associated with von Willebrand disease in two Chinese patients.

Wang, Yaqin; Wang, Xiong; Lu, Yanjun; Zhang, Ai; Yu, Wen; Hu, Qun; Liu, Aiguo; Huang, Jin-Feng

Wang, Yaqin; Wang, Xiong; Lu, Yanjun; Zhang, Ai; Yu, Wen; Hu, Qun; Liu, Aiguo; Huang, Jin-Feng.

Afiliación

Wang Y; Department of Pediatrics.
Wang X; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan.
Lu Y; Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan.
Zhang A; Department of Pediatrics.
Yu W; Department of Pediatrics.
Hu Q; Department of Pediatrics.
Liu A; Department of Pediatrics.
Huang JF; Department of Medical Genetics, Naval Medical University, Shanghai; Department of Clinical Genetics, Changhai Hospital, Naval Medical University, Shanghai, PR China.

Blood Coagul Fibrinolysis ; 34(1): 33-39, 2023 Jan 01.

Article en En | MEDLINE | ID: mdl-36598376

Asunto(s)

Hemostáticos; Enfermedades de von Willebrand; Niño; Humanos; Pueblos del Este de Asia; Factor VIII/genética; Hemorragia; Enfermedades de von Willebrand/genética; Factor de von Willebrand/genética

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades de von Willebrand / Hemostáticos Tipo de estudio: Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Blood Coagul Fibrinolysis Asunto de la revista: ANGIOLOGIA / HEMATOLOGIA Año: 2023 Tipo del documento: Article

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