Associated Papers
Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to Families.
Kotta MC et al.
Journal of the American Heart Association, 2023
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes.
Yoneda ZT et al.
Jama Cardiology, 2021
34495297 (PubMed )
Supplement: jamacardiol-e213370-s001.pdf
A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death.
Chanavat V et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2016
Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies.
Millat G et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2014
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathy.
Millat G et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2010
Results of comprehensive diagnostic work-up in 'idiopathic' dilated cardiomyopathy.
Broch K et al.
Open Heart, 0
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