Cargando…
PRDM16, LRP1 and TRPM8 genetic polymorphisms are risk factor for Pakistani migraine patients
BACKGROUND: Migraine is a chronic neurovascular condition characterized by recurring attacks of pulsating headaches. Genome-wide association studies (GWAS) identified many potential loci associated with migraine. To check the association of polymorphisms of PRDM16 (rs2651899), LRP1 (rs11172113), and...
Autores principales: | Zafar, R., Saleem, T., Sheikh, N., Maqbool, H., Mukhtar, M., Abbasi, M.H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459056/ https://www.ncbi.nlm.nih.gov/pubmed/34588893 http://dx.doi.org/10.1016/j.sjbs.2021.06.028 |
Ejemplares similares
-
GABRG2 C588T Polymorphism Is Associated with Idiopathic Generalized Epilepsy but Not with Antiepileptic Drug Resistance in Pakistani Cohort
por: Saleem, Tayyaba, et al.
Publicado: (2022) -
Association of ACE Gene I/D polymorphism with migraine in Kashmiri population
por: Wani, Irfan Yousuf, et al.
Publicado: (2016) -
Development of TRPM8 Antagonists to Treat Chronic Pain and Migraine
por: Weyer, Andy D., et al.
Publicado: (2017) -
TRPM8 genetic variant is associated with chronic migraine and allodynia
por: Ling, Yu-Hsiang, et al.
Publicado: (2019) -
PRDM16 Gene Polymorphism Is Associated with Obesity and Blood Lipids Profiles in Saudi Population
por: AlAmrani, Aishah, et al.
Publicado: (2018)