Cargando…
Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis
OBJECTIVE: Primary progressive multiple sclerosis (PPMS) causes accumulation of neurological disability from disease onset without clinical attacks typical of relapsing multiple sclerosis (RMS). However, whether genetic variation influences the disease course remains unclear. We aimed to determine w...
Autores principales: | Jia, Xiaoming, Madireddy, Lohith, Caillier, Stacy, Santaniello, Adam, Esposito, Federica, Comi, Giancarlo, Stuve, Olaf, Zhou, Yuan, Taylor, Bruce, Kilpatrick, Trevor, Martinelli‐Boneschi, Filippo, Cree, Bruce A.C., Oksenberg, Jorge R., Hauser, Stephen L., Baranzini, Sergio E |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119489/ https://www.ncbi.nlm.nih.gov/pubmed/29908077 http://dx.doi.org/10.1002/ana.25263 |
Ejemplares similares
-
Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset
por: Khankhanian, Pouya, et al.
Publicado: (2010) -
In depth comparison of an individual’s DNA and its lymphoblastoid cell line using whole genome sequencing
por: Nickles, Dorothee, et al.
Publicado: (2012) -
Genetic contribution to multiple sclerosis risk among Ashkenazi Jews
por: Khankhanian, Pouya, et al.
Publicado: (2015) -
Specific hypomethylation programs underpin B cell activation in early multiple sclerosis
por: Ma, Qin, et al.
Publicado: (2021) -
Integration of epigenetic and genetic profiles identifies multiple sclerosis disease-critical cell types and genes
por: Ma, Qin, et al.
Publicado: (2023)