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Updated: Dec 20, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Association of uncoupling protein (Ucp) gene polymorphisms with cardiometabolic diseases

Anna E Pravednikova1,2, Sergey Y Shevchenko1, Victor V Kerchev2

  • 1Laboratory of Gene Expression Regulation in Development, Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.

Molecular Medicine (Cambridge, Mass.)
|May 27, 2020
PubMed

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