Association of STin2 VNTR Polymorphism in the SLC6A4 Gene with Increased Risk of MS Disease
Author(s) -
Sahar Esfandiary,
Parisa Mohamadynejad,
Mohamad Mehdi Moghani Bashi
Publication year - 2019
Publication title -
alborz university medical journal
Language(s) - English
Resource type - Journals
eISSN - 2588-3046
pISSN - 2322-3839
DOI - 10.29252/aums.8.4.317
Subject(s) - serotonin transporter , serotonin , disease , pathogenesis , multiple sclerosis , biology , serotonergic , genotype , medicine , neuroscience , gene , genetics , immunology , receptor
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