Title : New familial heterozygous c 4066_4068 delTT 2 bp deletion of the SCN5A gene causing Brugada syndrome.

Pub. Date : 2011 Aug

PMID : 21397042






1 Functional Relationships(s)
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1 CONCLUSION: We describe a family partly with Brugada syndrome and a novel mutation in the exon 23 of the SCN5A gene leading to a deletion of 2 thymidine bases. Thymidine sodium voltage-gated channel alpha subunit 5 Homo sapiens