Pathogenesis of Unexplained Drowning: New Insights From a Molecular Autopsy
- 1 May 2005
- journal article
- case report
- Published by Elsevier in Mayo Clinic Proceedings
- Vol. 80 (5) , 596-600
- https://doi.org/10.4065/80.5.596
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Cardiac channelopathies: it's in the genesNature Medicine, 2004
- Prevention of Drowning in Infants, Children, and AdolescentsPediatrics, 2003
- Molecular and Cellular Mechanisms of Cardiac ArrhythmiasCell, 2001
- Molecular Diagnosis of the Inherited Long-QT Syndrome in a Woman Who Died after Near-DrowningNew England Journal of Medicine, 1999
- The Long QT Syndrome: Ion Channel Diseases of the HeartMayo Clinic Proceedings, 1998
- Mutations in the hminK gene cause long QT syndrome and suppress lKs functionNature Genetics, 1997
- Ion Channels — Basic Science and Clinical DiseaseNew England Journal of Medicine, 1997
- Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmiasNature Genetics, 1996
- SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndromeCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995