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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الحاوية / القاعدة:	Frontiers in Cardiovascular Medicine
المؤلفون الرئيسيون:	Nikki van der Velde, Roy Huurman, H. Carlijne Hassing, Ricardo P. J. Budde, Marjon A. van Slegtenhorst, Judith M. A. Verhagen, Arend F. L. Schinkel, Michelle Michels, Alexander Hirsch
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	Frontiers Media S.A. 2021-09-01
الموضوعات:	hypertrophic cardiomyopathy cardiovascular magnetic resonance sarcomere gene variants morphological features genotype risk prediction
الوصول للمادة أونلاين:	https://www.frontiersin.org/articles/10.3389/fcvm.2021.727405/full