FLNC missense variants in familial noncompaction cardiomyopathy

FLNC missense variants in familial noncompaction cardiomyopathy

The majority of familial noncompaction cardiomyopathy (NCCM) is explained by pathogenic variants in the same sarcomeric genes that are associated with hypertrophic (HCM) and dilated (DCM) cardiomyopathy. Pathogenic variants in the filamin C gene (FLNC) have been linked to HCM and DCM. We expand the...

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Bibliographic Details
Main Authors: Jaap I. van Waning, Yvonne M. Hoedemaekers, Wouter P. te Rijdt, Arne I. Jpma, Daphne Heijsman, Kadir Caliskan, Elke S. Hoendermis, Tineke P. Willems, Arthur van den Wijngaard, Albert Suurmeijer, Marjon A. van Slegtenhorst, Jan D.H. Jongbloed, Danielle F. Majoor-Krakauer, Paul A. van der Zwaag
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Cardiogenetics
Online Access:https://pagepressjournals.com/index.php/cardiogen/article/view/8181

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https://pagepressjournals.com/index.php/cardiogen/article/view/8181

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