Article
[Association of Polymorphic Genome Variants in the 2q32.1 Locus with the Development of Vasovagal Syncope].
Molekuliarnaia biologiia - 1 Jan 2023
Matveeva N A, Titov B V, Bazyleva E A, Kuchinskaya E A, Kozin M S, Favorov A V, Pevzner A V, Favorova O O
Abstract excerpt
The vasovagal syncope (VVS) is the most common form of syncope. The mechanisms of VVS development are not entirely clear. It is known that there is a genetic predisposition to this disease, but the data on the roles of individual genes are quite contradictory. Recently, a genome-wide association study identified a locus at chromosome 2q32.1 associated with a united group of diseases, that is, syncope and...
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