A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency.

Chang, Yueh-Shih; Lan, Yi-Cheng; Chen, Ya-Jyun; Huang, Jen-Seng; Yang, Chia-Ning; Huang, Chi-Ying F; Yeh, Kun-Yun

Chang, Yueh-Shih; Lan, Yi-Cheng; Chen, Ya-Jyun; Huang, Jen-Seng; Yang, Chia-Ning; Huang, Chi-Ying F; Yeh, Kun-Yun.

Afiliação

Chang YS; Division of Hemato-Oncology, Department of Internal Medicine, College of Medicine, Chang Gung Memorial Hospital, Keelung & Chang Gung University, Keelung, Taiwan.
Lan YC; Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
Chen YJ; Division of Hemato-Oncology, Department of Internal Medicine, College of Medicine, Chang Gung Memorial Hospital, Keelung & Chang Gung University, Keelung, Taiwan.
Huang JS; Institute of Precision Medicine, National Sun Yat-sen University, Kaohsiung, Taiwan.
Yang CN; Division of Hemato-Oncology, Department of Internal Medicine, College of Medicine, Chang Gung Memorial Hospital, Keelung & Chang Gung University, Keelung, Taiwan.
Huang CF; Institute of Precision Medicine, National Sun Yat-sen University, Kaohsiung, Taiwan.
Yeh KY; Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.

Front Med (Lausanne) ; 9: 870269, 2022.

Article em En | MEDLINE | ID: mdl-35755047

Palavras-chave

Asia; coagulopathy; factor V deficiency; factor V gene; polymorphism

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Med (Lausanne) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Taiwan

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