Novel Morphological Features on CMR for the Prediction of Pathogenic Sarcomere Gene Variants in Subjects Without Hypertrophic Cardiomyopathy

Background: Carriers of pathogenic DNA variants (G+) causing hypertrophic cardiomyopathy (HCM) can be identified by genetic testing. Several abnormalities have been brought forth as pre-clinical expressions of HCM, some of which can be identified by cardiovascular magnetic resonance (CMR). In this s...

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Detalles Bibliográficos
Autores principales: van der Velde, Nikki, Huurman, Roy, Hassing, H. Carlijne, Budde, Ricardo P. J., van Slegtenhorst, Marjon A., Verhagen, Judith M. A., Schinkel, Arend F. L., Michels, Michelle, Hirsch, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484536/
https://www.ncbi.nlm.nih.gov/pubmed/34604355
http://dx.doi.org/10.3389/fcvm.2021.727405

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484536/
https://www.ncbi.nlm.nih.gov/pubmed/34604355
http://dx.doi.org/10.3389/fcvm.2021.727405

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