The Association Between STX1B Polymorphisms and Treatment Response in Patients With Epilepsy

Background: Epilepsy is a debilitating brain disease with complex inheritance and frequent treatment resistance. However, the role of STX1B single nucleotide polymorphisms (SNPs) in epilepsy treatment remains unknown. Objective: This study aimed to explore the genetic association of STX1B SNPs with...

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Detalles Bibliográficos
Autores principales: Wang, Shitao, Zhou, Liang, He, Chenglu, Wang, Dan, Cai, Xuemei, Yu, Yanying, Chen, Liling, Lu, Di, Bian, Ligong, Du, Sunbing, Wu, Qian, Han, Yanbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299048/
https://www.ncbi.nlm.nih.gov/pubmed/34305610
http://dx.doi.org/10.3389/fphar.2021.701575

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299048/
https://www.ncbi.nlm.nih.gov/pubmed/34305610
http://dx.doi.org/10.3389/fphar.2021.701575

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