Genomic and Molecular Cardiology
Genomic and Molecular Cardiology MS001-2018
Brugada syndrome is a genetic condition that predisposes to ventricular tachycardia. It is caused by loss of function heterozygous mutations of the SCN5A gene in 20% of patients with the condition. There is only a single report of Brugada syndrome due to a large deletion involving the whole of SCN5A in the literature. We describe a further two families with identical chromosome 3p22.2 deletions including the SCN5A and SCN10A genes only. Read more
Seminars in Genomic and Precision Medicine
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