Homozygous SPEG Mutation Is Associated With Isolated Dilated Cardiomyopathy
- 1 April 2021
- journal article
- letter
- Published by Wolters Kluwer Health in Circulation: Genomic and Precision Medicine
- Vol. 14 (2) , 255-257
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- A Novel Recessive Mutation in SPEG Causes Early Onset Dilated CardiomyopathyPLOS Genetics, 2020
- Novel SPEG variant cause centronuclear myopathy in ChinaJournal of Clinical Laboratory Analysis, 2019
- SPEG Controls Calcium Reuptake Into the Sarcoplasmic Reticulum Through Regulating SERCA2a by Its Second Kinase-DomainCirculation Research, 2019
- SPEG (Striated Muscle Preferentially Expressed Protein Kinase) Is Essential for Cardiac Function by Regulating Junctional Membrane Complex ActivityCirculation Research, 2017
- SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated CardiomyopathyThe American Journal of Human Genetics, 2014