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Cardiac Filaminopathies: illuminating the divergent role of Filamin C mutations in human cardiomyopathy

Over the past decades, there has been tremendous progress in understanding genetic alterations that can result in different phenotypes of human cardiomyopathies. More than a thousand mutations in various genes have been identified, indicating that distinct genetic alterations, or combinations of gen...

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Bibliographic Details
Main Authors: Eden, Matthias (Author) , Frey, Norbert (Author)
Format: Article (Journal)
Language:English
Published: 4 February 2021
In: Journal of Clinical Medicine
Year: 2021, Volume: 10, Issue: 4, Pages: 1-8
ISSN:2077-0383
DOI:10.3390/jcm10040577
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/jcm10040577
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2077-0383/10/4/577
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Author Notes:Matthias Eden, Norbert Frey

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