Analysis of the Allele Polymorphism of (CTG)nand (CAG)n Triplet Repeats in Loci DM, DRPLA, and SCA1 in Several Populations of Russia |
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Authors: | S. N. Popova P. A. Slominsky S. N. Galushkin L. A. Tarskaya V. A. Spitsyn I. A. Guseva S. A. Limborska |
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Affiliation: | (1) Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, 123182, Russia;(2) Department of Anthropology, Moscow State University, Moscow, 119899, Russia;(3) Medical Genetic Research Center, Russian Academy of Medical Sciences, Moscow, 115475, Russia;(4) Institute of Rheumatology, Russian Academy of Medical Sciences, Moscow, 115470, Russia |
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Abstract: | ![]() Polymorphism of highly polymorphic triplet repeats CTG of the 3"-untranslated region of the myotonin protein kinase gene and CAG of the genes associated with dentatorubral-pallidoluysian atrophy (DRPLA, or Hew River syndrome) and spinocerebellar ataxia type 1 (SCA1) was analyzed in several ethnic populations of Russia. A difference in allele spectra of the three genes was demonstrated for populations differing in ethnic origin. |
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