Four novel SCN5A mutations in patients with Brugada syndrome

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Authors	BÉBAROVÁ Markéta JONGBLOED Roselie GEELEN Jan TIMMERMANS Carl ARENS Yvonne VOLDERS Paul RODRIGUEZ Luz-Maria
Year of publication	2006
Type	Conference abstract
MU Faculty or unit	Faculty of Medicine
Citation
Description	Four novel mutation in the SCN5A gene,coding the alpha-subunit of sodium channel, were detected in patients with Brugada syndrome.
Related projects:	Early diagnostics and treatment of cardiovascular diseases