Association of Multiple Sclerosis Phenotypes with Single Nucleotide Polymorphisms of IL7R, LAG3, and CD40 Genes in a Jordanian Population: A Genotype-Phenotype Study

It is thought that genetic variations play a vital role in the Multiple Sclerosis (MS) etiology. However, the role of genetic factors that influence the clinical features of MS remains unclear. We investigated the correlation between 21 single nucleotide polymorphisms within three genes (IL7R, LAG3,...

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Detalles Bibliográficos
Autores principales: AL-Eitan, Laith, Al Qudah, Malak, Al Qawasmeh, Majdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175123/
https://www.ncbi.nlm.nih.gov/pubmed/32111053
http://dx.doi.org/10.3390/biom10030356

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175123/
https://www.ncbi.nlm.nih.gov/pubmed/32111053
http://dx.doi.org/10.3390/biom10030356

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