Genome-Wide Association Identifies a Deletion in the 3′ Untranslated Region of Striatin in a Canine Model of Arrhythmogenic Right Ventricular Cardiomyopathy

Human Genetics - Germany
doi 10.1007/s00439-010-0855-y
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Arrhythmogenic Right Ventricular Cardiomyopathy

Heart
Cardiovascular MedicineCardiology
2004English

Echocardiographic Assessment of Arrhythmogenic Right Ventricular Cardiomyopathy

Heart
2001English

Signs of Right Ventricular Myocyte Hypertrophy in Arrhythmogenic Cardiomyopathy

Health and Primary Care
2019English

Arrhythmogenic Right Ventricular Cardiomyopathy: An Update

Heart
Cardiovascular MedicineCardiology
2009English

Arrhythmogenic Right Ventricular Cardiomyopathy: A Cause of Sudden Death in Young People.

Cleveland Clinic Journal of Medicine
Medicine
2001English

CARDIOMYOPATHY: Arrhythmogenic Right Ventricular Cardiomyopathy: Diagnosis, Prognosis, and Treatment

Heart
2000English

"Petrified" Right Ventricle in Long-Standing Naxos Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation
Cardiovascular MedicinePhysiologyCardiology
2001English

Congenital Partial Absence of Pericardium: A Mimic of Arrhythmogenic Right Ventricular Cardiomyopathy

Case Reports in Medicine
Medicine
2018English

Histology of Sudden Death in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia * Response

Circulation
Cardiovascular MedicinePhysiologyCardiology
2004English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy