Genetics of myasthenia gravis: a case-control association study in the Hellenic population.
Ontology highlight
ABSTRACT: Myasthenia gravis (MG) is an heterogeneous autoimmune disease characterized by the production of autoantibodies against proteins of the postsynaptic membrane, in the neuromuscular junction. The contribution of genetic factors to MG susceptibility has been evaluated through family and twin studies however, the precise genetic background of the disease remains elusive. We conducted a case-control association study in 101 unrelated MG patients of Hellenic origin and 101 healthy volunteers in order to assess the involvement of common genetic variants in susceptibility to MG. We focused on three candidate genes which have been clearly associated with several autoimmune diseases, aiming to investigate their potential implication in MG pathogenesis. These are interferon regulatory factor 5 (IRF-5
SUBMITTER: Zagoriti Z
PROVIDER: S-EPMC3463197 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature
ACCESS DATA