Associated Papers
MYH6 in Congenital Heart Defects: A Genotype-Phenotype Characterization in a French Cohort.
Daire E et al.
Pediatric Cardiology, 2025
Identification and genetic analysis of rare variants in myosin family genes in 412 Han Chinese congenital heart disease patients.
Zhang Y et al.
Molecular Genetics & Genomic Medicine, 2022
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
Mademont-Soler I et al.
Plos One, 2017
28771489 (PubMed )
Supplement: pone.0181465.s002.xlsx › Supplementary_Table_2
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