EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias
Article in European Journal of Human Genetics (July 2023)
The most recent citing publications are shown below. View all 22 publications that cite this research output on Dimensions.
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
Article in Orphanet Journal of Rare Diseases (January 2023)
Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1
Article in Journal of Cardiovascular Electrophysiology (December 2021)