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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Bibliografische gegevens
Gepubliceerd in:Pharmgenomics Pers Med
Hoofdauteurs: AL-Eitan, Laith N, Al-Dalalah, Islam M, Mustafa, Mohamed M, Alghamdi, Mansour A, Elshammari, Afrah K, Khreisat, Wael H, Aljamal, Hanan A
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Dove 2019
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Original Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6572658/
https://ncbi.nlm.nih.gov/pubmed/31354331
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PGPM.S211490
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