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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Bibliografske podrobnosti
izdano v: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.
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2016
Teme:
PRE-CLINICAL RESEARCH
Online dostop: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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