Inherited Cardiomyopathies: Genetics and Clinical Genetic Testing
Inherited cardiomyopathies are major causes of morbidity and mortality and include a group of cardiac disorders such as hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy, arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C), left ventricular noncompaction (LVNC), and restrictiv...
Main Authors: | Guoliang Wang, MD, PhD, Ruirui Ji, MD, PhD, Wenxin Zou, PhD, Daniel J. Penny, MD, PhD, Yuxin Fan, MD, PhD |
---|---|
Format: | Article |
Language: | English |
Published: |
Compuscript
2017-02-01
|
Series: | Cardiovascular Innovations and Applications |
Subjects: | |
Online Access: | http://www.ingentaconnect.com/content/cscript/cvia/2017/00000002/00000002/art00020 |
Similar Items
-
Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies
by: Andreas Brodehl, et al.
Published: (2019-09-01) -
Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies
by: Quynh Nguyen, et al.
Published: (2020-01-01) -
Genetic Counseling in Inherited Cardiomyopathies
by: Sarah Moharem-Elgamal, MD, PhD, et al.
Published: (2020-03-01) -
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) -
Thebesian Veins Draining to the Left Ventricle, Mimicking Left Ventricular Noncompaction
by: Simon F. Stämpfli, MD, MSc, et al.
Published: (2020-11-01)