Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes

Int J Cardiol. 2015 Apr 1:184:272-273. doi: 10.1016/j.ijcard.2015.02.029. Epub 2015 Feb 24.

Authors

Tatiana Pervunina¹, Tatiana Vershinina¹, Artem Kiselev¹, Irina Nikitina¹, Eugeniy Grekhov¹, Lubov Mitrofanova¹, Gunnar Sjoberg², Anna Kostareva³

Affiliations

¹ Almazov Federal Medical Research Center, St. Petersburg, Russia.
² Department of Women's and Children's Health, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
³ Almazov Federal Medical Research Center, St. Petersburg, Russia; Department of Women's and Children's Health, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden. Electronic address: anna.kostareva@ki.se.

PMID: 25731833
DOI: 10.1016/j.ijcard.2015.02.029

No abstract available

Keywords: Double mutation; Hypertrophic cardiomyopathy; Next generation sequencing; RAS-pathway.

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Cardiomyopathy, Hypertrophic / diagnosis*
Cardiomyopathy, Hypertrophic / genetics*
Cardiomyopathy, Hypertrophic / surgery
Genes, ras / genetics*
Humans
Infant
Male
Mutation / genetics*