MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy

Circ Genom Precis Med. 2021 Oct;14(5):e003476. doi: 10.1161/CIRCGEN.121.003476. Epub 2021 Sep 24.

¹ Instituto Nacional de Cardiologia, Rio de Janeiro, Brazil (G.M.D., M.S., A.C.C.d.C., F.E.S.C.F.).
² Universidade Estadual do Norte Fluminense Darcy Ribeiro, Brazil (G.M.D., E.M.-A.).
³ Health in Code SL, A Coruña, Spain (A.L.J.).
⁴ Universidade da Coruña, A Coruña, Spain (A.L.J.).
⁵ Lankenau Institute for Medical Research, Philadelphia (H.B.-M.).
⁶ Department of Chemistry, University of Mary, Bismarck (D.B.).
⁷ Biocor Instituto, Belo Horizonte, Brazil (E.B.S.).
⁸ Universidade Federal do Rio de Janeiro, Brazil (A.C.C.d.C.).
⁹ Instituto Nacional de Ciência e Tecnologia em Medicina Regenerativa, Brazil (A.C.C.d.C.).

No abstract available

Keywords: MYH7; genetic testing; genotype; heart failure; hypertrophic cardiomyopathy; phenotype.

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