The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders.

Gunathilake, K M D; Sirisena, U N D; Nisansala, P K D; Goonasekera, H W W; Jayasekara, R W; Dissanayake, V H W

Gunathilake, K M D; Sirisena, U N D; Nisansala, P K D; Goonasekera, H W W; Jayasekara, R W; Dissanayake, V H W.

Afiliación

Gunathilake KM; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.
Sirisena UN; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.
Nisansala PK; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.
Goonasekera HW; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.
Jayasekara RW; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.
Dissanayake VH; Human Genetics Unit, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 8, Sri Lanka.

Indian J Hematol Blood Transfus ; 31(3): 356-61, 2015 Sep.

Article en En | MEDLINE | ID: mdl-26085721

Palabras clave

F2 20210G>A; Prevalence; Prothrombin; Thrombophilia; Venous thrombo-embolic disorders

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prevalence_studies / Risk_factors_studies Idioma: En Revista: Indian J Hematol Blood Transfus Año: 2015 Tipo del documento: Article País de afiliación: Sri Lanka Pais de publicación: India

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