Effects of MTHFR and ABCC2 gene polymorphisms on antiepileptic drug responsiveness in Jordanian epileptic patients

BACKGROUND: Epilepsy is one of the most common neurological diseases with unclear etiology where its genetic background and treatment regime still need further exploration. OBJECTIVES: This study designed to evaluate the pharmacogenomics of MTHFR and ABCC2 genes, and their association with epilepsy...

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Detalles Bibliográficos
Autores principales: AL-Eitan, Laith N, Al-Dalalah, Islam M, Mustafa, Mohamed M, Alghamdi, Mansour A, Elshammari, Afrah K, Khreisat, Wael H, Aljamal, Hanan A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572658/
https://www.ncbi.nlm.nih.gov/pubmed/31354331
http://dx.doi.org/10.2147/PGPM.S211490

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572658/
https://www.ncbi.nlm.nih.gov/pubmed/31354331
http://dx.doi.org/10.2147/PGPM.S211490

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