Bases Moleculares de la Arteriosclerosis
CTS347
Catholic University of the Sacred Heart
Milán, ItaliaPublicaciones en colaboración con investigadores/as de Catholic University of the Sacred Heart (5)
2022
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Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
Human Genetics, Vol. 141, Núm. 10, pp. 1579-1589
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Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes
Journal of Personalized Medicine, Vol. 12, Núm. 2
2021
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Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later
Journal of Personalized Medicine, Vol. 11, Núm. 3, pp. 1-14
2020
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Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
EBioMedicine, Vol. 54
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Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Forensic Science International: Genetics, Vol. 47