Associated Papers
Atrial fibrillation-a complex polygenetic disease.
Andersen JH et al.
European Journal of Human Genetics : Ejhg, 2021
33279945 (PubMed )
Supplement: 41431_2020_784_MOESM3_ESM.xlsx › Sheet1
NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arteriosus.
Ritter A et al.
American Journal of Medical Genetics. Part A, 2020
NKX2-6 mutation predisposes to familial atrial fibrillation.
Wang J et al.
International Journal of Molecular Medicine, 2014
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