Associated Papers
Multiplexed Functional Assessments of MYH7 Variants in Human Cardiomyocytes.
Friedman CE et al.
Circulation. Genomic and Precision Medicine, 2024
A case of MYH7 and MYH9 genes variants with cardiomyopathy and macrothrombocytopenia.
Ikawa Y et al.
Clinical Case Reports, 2024
Shared Genetic Etiology of Primary Dilated Cardiomyopathy and Ischemic Dilated Cardiomyopathy.
Sun Y et al.
Frontiers in Cardiovascular Medicine, 2021
37273834 (PubMed )
Supplement: Data_Sheet_2.xlsx › Sheet1
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
Mademont-Soler I et al.
Plos One, 2017
Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.
Fujino N et al.
Clinical Cardiology, 2013
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