about
Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathyLarge Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients.The PRKAG2 gene and hypertrophic cardiomyopathy: an energetically imbalanced relationship.A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulationWhole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic CardiomyopathyChromatin remodelling and epigenetic state regulation by non-coding RNAs in the diseased heart.Metabolic Alterations in Inherited CardiomyopathiesMicroRNAs in Cardiac DiseasesA targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy
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Q27310698-1B4469CE-EC26-4622-88CB-239CA8F9C9E5Q47644282-A902080A-8154-48E1-A808-478484835354Q48261584-FEB6F207-A4B7-42BF-B66A-F01C2BDE0954Q57283062-B343E003-0445-4C09-8520-36B0DC11BD95Q57818782-46955C84-FC02-4739-8A4A-B0B3D8968761Q64904280-7109BD28-FBE5-48CA-A50A-A4A30ADF72E6Q92012621-227E79A5-6F35-41BF-B6FC-88E6DBAB4E9DQ92026116-78EA98BA-5F9A-4713-87A0-0BF90A1D9DB7Q93213387-2629B8BB-9C45-4209-B558-B16FDCBD08A2
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description
researcher (ORCID 0000-0003-4751-1476)
@en
name
M Calore
@en
type
label
M Calore
@en
prefLabel
M Calore
@en
P31
P496
0000-0003-4751-1476