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

The Genomic Medicine Foundation publishes its own journal reviews series ‘Seminars in Genomic and Precision Medicine’ providing cutting edge research and new developments in all aspects of genomics research relevant to medicine and health. All enquiries and submissions to this series please write to