SCN5A is a disease-causing gene associated with familial dilated cardiomyopathy (FDC). We examined the possible association between a common polymorphism in the SCN5A gene (c.1673A>G-p.H558R; rs1805124) and the risk of dilated cardiomyopathy (DCM) occurrence.
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy / Mazzaccara, Cristina; Limongelli, Giuseppe; Petretta, Mario; Vastarella, Rossella; Pacileo, Giuseppe; Bonaduce, Domenico; Salvatore, Francesco; Frisso, Giulia. - In: JOURNAL OF CARDIOVASCULAR MEDICINE. - ISSN 1558-2027. - 19:7(2018), pp. 344-350. [10.2459/JCM.0000000000000670]
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy
Mazzaccara, Cristina;Petretta, MarioWriting – Review & Editing
;Bonaduce, Domenico;Salvatore, Francesco
;Frisso, Giulia
2018
Abstract
SCN5A is a disease-causing gene associated with familial dilated cardiomyopathy (FDC). We examined the possible association between a common polymorphism in the SCN5A gene (c.1673A>G-p.H558R; rs1805124) and the risk of dilated cardiomyopathy (DCM) occurrence.File in questo prodotto:
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