Cargando…
DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder. Missense mutations of DCTN1 have been identified as a possible genetic risk factor for ALS. Here, we tested the DCTN1 protein-coding exons in 510 sporadic ALS patients in whom SOD1, TARDBP, FUS, and C9orf72 genes were screene...
Autores principales: | Liu, Xiangyi, Yang, Lipeng, Tang, Lu, Chen, Lu, Liu, Xiaolu, Fan, Dongsheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549744/ https://www.ncbi.nlm.nih.gov/pubmed/28792508 http://dx.doi.org/10.1371/journal.pone.0182572 |
Ejemplares similares
-
Analysis of ERBB4 Variants in Amyotrophic Lateral Sclerosis Within a Chinese Cohort
por: Wang, Fan, et al.
Publicado: (2022) -
The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis
por: Xu, Lianping, et al.
Publicado: (2017) -
Long-Term Use of Riluzole Could Improve the Prognosis of Sporadic Amyotrophic Lateral Sclerosis Patients: A Real-World Cohort Study in China
por: Chen, Lu, et al.
Publicado: (2016) -
The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population
por: Xu, Lianping, et al.
Publicado: (2018) -
Cognitive Impairment in Chinese Patients with Sporadic Amyotrophic Lateral Sclerosis
por: Cui, Bo, et al.
Publicado: (2015)