A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family
Takanori Suzuki, Kazuyoshi Saito, Tetsushi Yoshikawa, Keichi Hirono, Yukiko Hata, Naoki Nishida, Kazushi Yasuda, Masami Nagashima
Topics & Concepts
MYH7Hypertrophic cardiomyopathyMYH6Missense mutationFrameshift mutationGeneticsPhenotypeGenetic heterogeneityGeneInternal medicineMedicineBiologyGene isoformCardiomyopathy and Myosin StudiesCongenital heart defects researchWilliams Syndrome Research