Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.
Dilated cardiomyopathy, a major cause of chronic heart failure and cardiac transplantation, is characterized by left ventricular or biventricular heart dilatation. In nearly 50% of cases the pathology is inherited, and more than 60 genes have been reported as disease-causing. However, in 30% of fami...
Main Authors: | Rocio Toro, Alexandra Pérez-Serra, Oscar Campuzano, Javier Moncayo-Arlandi, Catarina Allegue, Anna Iglesias, Alipio Mangas, Ramon Brugada |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2016-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC4938129?pdf=render |
Similar Items
-
Plasma microrna expression profile for reduced ejection fraction in dilated cardiomyopathy
by: Maria Calderon-Dominguez, et al.
Published: (2021-04-01) -
A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy
by: Jun Guo, et al.
Published: (2019-08-01) -
Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies
by: Oscar Campuzano, et al.
Published: (2019-05-01) -
Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel <i>TTN</i> Frameshift Mutation
by: Emanuele Micaglio, et al.
Published: (2021-01-01) -
Genetic basis of atrial fibrillation
by: Oscar Campuzano, et al.
Published: (2016-12-01)