Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotype Margarida Oliveira, Olga Azevedo, Bebiana Faria, Pedro von Hafe, Geraldo Dias, Ricardo Faria, Victor Sanfins, Mário Lourenço, Gabriel Miltenberger-Miltenyi, António Lourenço

Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy Alexandra Toste, Andreas Perrot, Cemil Özcelik, Nuno Cardim

Complex phenotype linked to a mutation in exon 11 of the lamin A/C gene: Hypertrophic cardiomyopathy, atrioventricular block, severe dyslipidemia and diabetes Ana Rita G. Francisco, Inês Santos Gonçalves, Fátima Veiga, Mónica Mendes Pedro, Fausto J. Pinto, Dulce Brito