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Prevalent function of genome loci associated with development of multiple sclerosis as revealed by GWAS and eQTL analysis
Bykadorov P.A., Oparina N.Y., Fridman M.V., Makeev V.Y.
Carriage of 2R allele at VNTR polymorphous site of XRCC5 gene increases risk of multiple sclerosis in an Iranian population
Jahantigh D., Moghtaderi A., Narooie-Nejad M., Mousavi M., Moossavi M., Salimi S., Mohammadoo-Khorasani M.
Matrix Metalloproteinase-9 Gene Polymorphisms in South-West Iranian Multiple Sclerosis (MS) Patients
Sadr N.K., Galehdari H., Seifi T., Delfan N., Khatami S.R., Hafizi A.
Association between Allelic Variants of IL2, IL2RA, and IL7R Genes and Multiple Sclerosis
Timasheva Y.R., Zaplakhova O.V., Nasibullin T.R., Tuktarova I.A., Erdman V.V., Bakhtiiarova K.Z., Mustafina O.E.
Associations of Polymorphic DNA Markers and Their Combinations with Multiple Sclerosis
Zaplakhova O.V., Nasibullin T.R., Tuktarova I.A., Timasheva Y.R., Erdman V.V., Bakhtiyarova K.Z., Mustafina O.E.
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