A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy

AIMS: 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. METHODS: We genotyped 185 DCM c...

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Publicat a:J Cardiovasc Med (Hagerstown)
Autors principals: Mazzaccara, Cristina, Limongelli, Giuseppe, Petretta, Mario, Vastarella, Rossella, Pacileo, Giuseppe, Bonaduce, Domenico, Salvatore, Francesco, Frisso, Giulia
Format: Artigo
Idioma:Inglês
Publicat: Lippincott Williams & Wilkins 2018
Matèries:
Research articles: Heart failure
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6012048/
https://ncbi.nlm.nih.gov/pubmed/29782370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2459/JCM.0000000000000670
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