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Left ventricular cardiomyopathy due to CPT II hereditary deficiency. Keys to an infrequent diagnosis
Miocardiopatia ventricular esquerda por deficiência hereditária CPT II. Chaves para um diagnóstico pouco frequente
Lorena Herradora,b, Elena García Arumic, Fernando de Frutosa,b,
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fdefrutos@alumni.unav.es

Corresponding author.
a Cardiology Department, Bellvitge University Hospital, L’Hospitalet de Llobregat, Barcelona, Spain
b Bioheart Group, Cardiovascular, Respiratory and Systemic Diseases and Cellular Aging Program, Institut d’Investigació Biomèdica de Bellvitge (IDIBELL), L’Hospitalet de Llobregat, Barcelona, Spain
c Genetics Department, Vall d’Hebron University Hospital, Barcelona, Spain
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ISSN: 08702551
Original language: English plumx
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Revista Portuguesa de Cardiologia (English edition)