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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
PRE-CLINICAL RESEARCH
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5166708/
https://www.ncbi.nlm.nih.gov/pubmed/28008423
http://dx.doi.org/10.1016/j.jacbts.2016.05.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5166708/
https://www.ncbi.nlm.nih.gov/pubmed/28008423
http://dx.doi.org/10.1016/j.jacbts.2016.05.004

Ejemplares similares