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The Importance of Family-genetic Screening: The Phenotype Caused by the p.L3778F Ryanodine Receptor Mutation is Likely Less Severe Than Previously Thought.

Revista espanola de cardiologia (English ed.) - 1 Jul 2016

Groba-Marco María Del Val, Benito-Bartolomé Fernando, García-Aguado Marcos, García-Hernández Irene, Gimeno-Blanes Juan Ramón, Barriales-Villa Roberto

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PMID: 27198127
DOI: 10.1016/j.rec.2016.04.007

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