Associated Papers
Rare damaging variants in the sex differences of congenital heart disease: an exome sequencing study.
Sun H et al.
Ebiomedicine, 2025
40347836 (PubMed )
Supplement: mmc2.xlsx › Supplementary_Table_6
ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features.
Çağlayan AO et al.
Cold Spring Harbor Molecular Case Studies, 2017
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