FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy

A genetic etiology has been identified in 30% to 40% of dilated cardiomyopathy (DCM) patients, yet only 50% of these cases are associated with a known causative gene variant. Thus, in order to understand the pathophysiology of DCM, it is necessary to identify and characterize additional genes. In th...

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Bibliographische Detailangaben
Veröffentlicht in:JACC Basic Transl Sci
Hauptverfasser: Begay, Rene L., Tharp, Charles A., Martin, August, Graw, Sharon L., Sinagra, Gianfranco, Miani, Daniela, Sweet, Mary E., Slavov, Dobromir B., Stafford, Neil, Zeller, Molly J., Alnefaie, Rasha, Rowland, Teisha J., Brun, Francesca, Jones, Kenneth L., Gowan, Katherine, Mestroni, Luisa, Garrity, Deborah M., Taylor, Matthew R.G.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2016
Schlagworte:
PRE-CLINICAL RESEARCH
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5166708/
https://ncbi.nlm.nih.gov/pubmed/28008423
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacbts.2016.05.004
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