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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Detalles Bibliográficos
Publicado en:JACC Basic Transl Sci
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 2016
Assuntos:
PRE-CLINICAL RESEARCH
Acceso en liña: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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