Autor:	S. N. Galushkin, L. A. Tarskaya, Popova Sn, P. A. Slominsky, V. A. Spitsyn, Svetlana A. Limborska, I. A. Guseva
Rok vydání:	2002
Předmět:	Genetics congenital hereditary and neonatal diseases and abnormalities Spinocerebellar Ataxia Type 1 Myotonin-protein kinase Ethnic origin Biology medicine.disease Human genetics nervous system diseases Atrophy Polymorphism (computer science) medicine Allele Gene
Zdroj:	Russian Journal of Genetics. 38:1312-1315
ISSN:	1022-7954
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ca59761482a04713f7d794a498707cd4 https://doi.org/10.1023/a:1021159413816 Zobrazit plný text záznamu Full text from SpringerLink