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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Bibliografiska uppgifter
I publikationen:JACC Basic Transl Sci
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2016
Ämnen:
PRE-CLINICAL RESEARCH
Länkar: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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