Associated Papers
Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy.
Allouba M et al.
European Heart Journal, 2023
37431535 (PubMed )
Supplement: ehad372_supplementary_data.zip › supplementary_tables_revised_version_Feb2023.xlsx › Table_S3
Rupture of Splenic Artery Aneurysm in Patient with ACTN2 Mutation.
Palughi M et al.
Journal of Clinical Medicine, 2023
Case Report: A novel EPAS1 mutation in a case of paraganglioma complicated with polycythemia and atrial septal defect.
Yang H et al.
Frontiers in Endocrinology, 2023
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