-sectional study approaches 30%. The 2007
Movement Disorder Society criteria and algorithm for the diagnosis
Khusnutdinova, E.K.,
Dzhemileva, L.U.,
Lobov, S.L.,
Kuznetzov, D.U.,
Nazirova, A.G.,
Nurgalina, E.M.,
Barashkov, N.A.,
Fedorova, S.A. (2017) is of particular interest, because its ethnic
populations mostly belong to the Turkic, Finno-Ugric, and Slavonic
Solovyev, A.V.,
Barashkov, N.A.,
Bady-Khoo, M.S.,
Zytsar, M.V.,
Posukh, O.L.,
Romanov, G.P.,
Rafailov, A.M.,
Sazonov, N.N.,
Alexeev, A.N.,
Dzhemileva, L.U.,
Khusnutdinova, E.K.,
Fedorova, S.A. (2017) homozygous for mutation c.-23+1G>A from six Eurasian
populations were reconstructed. The structure
-nucleotide polymorphism (SNP) rs2476601 was shown to be associated with JIA in different
populations, but according