Work

KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes

Year: 2002

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/342360

Authors: Gregor Andelfinger, Andrew R. Tapper, Richard C. Welch, Carlos G. Vanoye, Alfred L. George, D. Woodrow Benson

Institutions: Cincinnati Children's Hospital Medical Center, University of Cincinnati, Vanderbilt University

Language: English

Topic: Cardiac electrophysiology and arrhythmias

Subfield: Cardiology and Cardiovascular Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke

Awards: G13928274, G5545063918, Hereditary Defects in Human Sodium Channels, G5756326348, REGULATION OF NUCLEOTIDE BINDING TO ROMK KATP CHANNEL, MOLECULAR DETERMINANTS OF PEDIATRIC HEART DISEASE, G7814066881, G8785659295, Biology of Arrhythmia Susceptibility, G97814394

OpenAlex ID: W2017263107

FWCI: 7.069

Cites: 25

Cited by: 262

Related to: 10