Cargando…
The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis
OBJECTIVE: Multiple Sclerosis (MS) is a common disease of the central nervous system. The interaction between inflammatory and neurodegenerative processes typically results in irregular neurological disturbances followed by progressive disability. Mitochondrial dysfunction has been implicated in neu...
Autores principales: | KHATAMI, Mehri, HEIDARI, Mohammad Mehdi, MANSOURI, Reza, MOUSAVI, Fatemeh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Beheshti University of Medical Sciences
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322497/ https://www.ncbi.nlm.nih.gov/pubmed/25767537 |
Ejemplares similares
-
The POLG Gene Polymorphism in Iranian Varicocele-Associated Infertility Patients
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2012) -
Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2017) -
Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich’s Ataxia
por: HEIDARI, Mohammad Mehdi, et al.
Publicado: (2014) -
Mitochondrial Genetic Variation in Iranian Infertile Men
with Varicocele
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2016) -
The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study
por: Heidari, Mohammad Mehdi, et al.
Publicado: (2019)