Compound Heterozygous SCN5A Mutations in a Toddler - Are they Associated with a More Severe Phenotype?

Por Sacilotto, Luciana, Epifanio, Hindalis Ballesteros, Darrieux, Francisco Carlos da Costa, Wulkan, Fanny, Oliveira, Theo Gremen Mimary, Hachul, Denise Tessariol, Pereira, Alexandre da Costa, Scanavacca, Mauricio Ibrahim
Publicado no Arq Bras Cardiol (2017)