Mario Torrado
A Coruna, GA, Spain
Last Updated: 09/26/2026
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Found 10 publications
Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree.
Journal: Scientific reports
Published: November 25, 2021
A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndrome.
Journal: NPJ genomic medicine
Published: September 10, 2020
Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: May 13, 2020
A Pathogenic Galactosidase A Mutation Coexisting With an MYBPC3 Mutation in a Female Patient With Hypertrophic Cardiomyopathy.
Journal: The Canadian journal of cardiology
Published: June 17, 2019
A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome.
Journal: BioMed research international
Published: February 26, 2018
Interplay between cardiac transcription factors and non-coding RNAs in predisposing to atrial fibrillation.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: January 24, 2018
Myocardial transcription factors in diastolic dysfunction: clues for model systems and disease.
Journal: Heart failure reviews
Published: June 17, 2016
A MicroRNA-Transcription Factor Blueprint for Early Atrial Arrhythmogenic Remodeling.
Journal: BioMed research international
Published: February 20, 2015
In search of novel targets for heart disease: myocardin and myocardin-related transcriptional cofactors.
Journal: Biochemistry research international
Published: January 19, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026