MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.

M'barek, Lamia; Sakka, Salma; Meghdiche, Fatma; Turki, Dhaker; Maalla, Khadija; Dammak, Mariem; Kallel, Choumous; Mhiri, Chokri

M'barek, Lamia; Sakka, Salma; Meghdiche, Fatma; Turki, Dhaker; Maalla, Khadija; Dammak, Mariem; Kallel, Choumous; Mhiri, Chokri.

Afiliación

M'barek L; Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease (LR-12-SP-19), Habib Bourguiba University Hospital, University of Sfax, Sfax, Tunisia. lamiambarek4@gmail.com.
Sakka S; Clinical Investigation Center (CIC), Habib Bourguiba University Hospital, Sfax, Tunisia. lamiambarek4@gmail.com.
Meghdiche F; Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease (LR-12-SP-19), Habib Bourguiba University Hospital, University of Sfax, Sfax, Tunisia.
Turki D; Laboratory of Hematology, Habib Bourguiba University Hospital, University of Monastir, Monastir, Tunisia.
Maalla K; Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease (LR-12-SP-19), Habib Bourguiba University Hospital, University of Sfax, Sfax, Tunisia.
Dammak M; Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease (LR-12-SP-19), Habib Bourguiba University Hospital, University of Sfax, Sfax, Tunisia.
Kallel C; Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease (LR-12-SP-19), Habib Bourguiba University Hospital, University of Sfax, Sfax, Tunisia.
Mhiri C; Laboratory of Hematology, Habib Bourguiba University Hospital, University of Monastir, Monastir, Tunisia.

Metab Brain Dis ; 36(3): 421-428, 2021 03.

Article en En | MEDLINE | ID: mdl-33400068

Asunto(s)

Factor V/genética; Accidente Cerebrovascular Isquémico/genética; Metilenotetrahidrofolato Reductasa (NADPH2)/genética; Mutación; Polimorfismo de Nucleótido Simple; Protrombina/genética; Adolescente; Adulto; Femenino; Predisposición Genética a la Enfermedad; Genotipo; Humanos; Masculino; Persona de Mediana Edad; Túnez; Adulto Joven

Palabras clave

Arterial ischemic stroke; Factor V leiden; MTHFR A1298C; MTHFR C677T; Prothrombin G20210A mutation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor V / Protrombina / Polimorfismo de Nucleótido Simple / Metilenotetrahidrofolato Reductasa (NADPH2) / Accidente Cerebrovascular Isquémico / Mutación Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: Metab Brain Dis Asunto de la revista: CEREBRO / METABOLISMO Año: 2021 Tipo del documento: Article País de afiliación: Túnez

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