FGF12 is a candidate Brugada syndrome locus

BACKGROUND: Less than 30% of the cases of Brugada syndrome (BrS) have an identified genetic cause. Of the known BrS-susceptibility genes, loss-of-function mutations in SCN5A or CACNA1C and their auxiliary subunits are most common. On the basis of the recent demonstration that fibroblast growth facto...

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Detalhes bibliográficos
Main Authors: Hennessey, Jessica A., Marcou, Cherisse A., Wang, Chuan, Wei, Eric Q., Wang, Chaojian, Tester, David J., Torchio, Margherita, Dagradi, Federica, Crotti, Lia, Schwartz, Peter J., Ackerman, Michael J., Pitt, Geoffrey S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3870051/
https://ncbi.nlm.nih.gov/pubmed/24096171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2013.09.064
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