Genetic testing for channelopathies, more than ten years progress and remaining challenges

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Genetic testing for channelopathies, more than ten years progress and remaining challenges

47 J Cardiovasc. Dis. Res. Vol. 1 / No 2 in 1996,[4] the identifi cation of mutations and investigation of genotype-phenotype relationships of channelopathies have become focal points in the fi eld of genetics and cardiology. For Brugada syndrome alone, 7 related genes, and hundreds of associated mutations have been identifi ed.[5,6] SCN5A, encoding the Nav1.5 α-subunit, causes the sodium ion c...

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ژورنال

عنوان ژورنال: Journal of Cardiovascular Disease Research

سال: 2010

ISSN: 0975-3583

DOI: 10.4103/0975-3583.64429