Associated Papers
Two Novel Functional Mutations in Promoter Region of SCN3B Gene Associated with Atrial Fibrillation.
Lin L et al.
Life (basel, Switzerland), 2022
Transcriptional factors in calcium mishandling and atrial fibrillation development.
Dai W et al.
Pflugers Archiv : European Journal of Physiology, 2021
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
In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease.
Abbasi S et al.
Journal of Cardiovascular and Thoracic Research, 2021
A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.
Zhang X et al.
Plos One, 2016
27391137 (PubMed )
Supplement: pone.0158904.s003.pdf
Atrial fibrillation: the role of common and rare genetic variants.
Olesen MS et al.
European Journal of Human Genetics : Ejhg, 2014
Identification of functional mutations in GATA4 in patients with congenital heart disease.
Wang E et al.
Plos One, 2013
23626780 (PubMed )
Supplement: pone.0062138.s004.xlsx › information_of_all_mutations
Novel GATA4 mutations in lone atrial fibrillation.
Jiang JQ et al.
International Journal of Molecular Medicine, 2011
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