Review Article
The contribution of genetics to the understanding and management of cardiomyopathies: Part 2
O contributo da genética para a compreensão das miocardiopatias: Parte 2
Isabel Cardosoa,b,
, Mafalda Meloc, Pedro Brása,b, José Miguel Viegasa,b, Inês Almeidaa,b, Sofia Nunesc, Inês Custódioc, Conceição Trigod,e, Sérgio Laranjod,e, Rafael Graçaf, Rui Cruz Ferreiraa,b, Mário Oliveirag,h,i,j,k, Sílvia Aguiar Rosaa,b,g,h, Diana Antunesc,f
Autor para correspondência
a Serviço de Cardiologia, Centro de Referência de Cardiopatias Miocardiopatias do Centro Hospitalar Universitário de Lisboa Central (CHULC), Santa Marta Hospital, CHULC, EPE, Lisboa, Portugal
b Member of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart, Centro Clínico Académico de Lisboa, Lisboa, Portugal
c Medical Genetics Department, Dona Estefânia Hospital, Central Lisbon Hospital and University Centre, Lisbon, Portugal
d Serviço de Cardiologia Pediátrica, Centro de Referência de Cardiopatias Congénitas do CHULC, Hospital de Santa Marta, CHULC, EPE, Lisboa, Portugal
e Member of the European Reference Network Guard-Heart, Centro Clínico Académico de Lisboa, Lisboa, Portugal
f GenoMed – Diagnósticos de Medicina Molecular, Instituto de Medicina Molecular, Lisbon, Portugal
g CHRC, NOVA Medical School, Faculdade de Ciências Médicas, NMS, FCM, Universidade Nova de Lisboa, Lisboa, Portugal
h Centro Clínico Académico de Lisboa, Lisboa, Portugal
i Arrhythmology, Pacing and Electrophysiology Unit, Cardiology Service, CHLC, Lisbon, Portugal
j Institute of Physiology and CCUL, Faculty of Medicine of Lisbon, Portugal
k Cardiology Center, Hospital CUF Tejo, Lisbon, Portugal
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