Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome
- 1 March 1998
- journal article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 6 (2), 129-133
- https://doi.org/10.1038/sj.ejhg.5200165