KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes
- 1 September 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (3) , 663-668
- https://doi.org/10.1086/342360
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Sex, hormones, and repolarizationCardiovascular Research, 2002
- Gender differences in arrhythmiasClinical Cardiology, 2002
- A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from IsraelAmerican Journal of Human Genetics, 2001
- The consequences of disrupting cardiac inwardly rectifying K+ current (IK1) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genesThe Journal of Physiology, 2001
- Andersen's syndrome: A distinct periodic paralysisAnnals of Neurology, 1997
- Ontogeny of Gene Expression of Kir Channel Subunits in the RatMolecular and Cellular Neuroscience, 1997
- Regions Responsible for the Assembly of Inwardly Rectifying Potassium ChannelsCell, 1996
- A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiationNature Genetics, 1995
- Primary structure and functional expression of a mouse inward rectifier potassium channelNature, 1993
- INTERMITTENT MUSCULAR WEAKNESS, EXTRASYSTOLES, AND MULTIPLE DEVELOPMENTAL ANOMALIESActa Paediatrica, 1971