Unraveling Monogenic Channelopathies and Their Implications for Complex Polygenic Disease
- 30 April 2003
- journal article
- review article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (4) , 785-803
- https://doi.org/10.1086/374317
Abstract
No abstract availableKeywords
This publication has 113 references indexed in Scilit:
- Novel truncated isoform of SK3 potassium channel is a potent dominant-negative regulator of SK currents: implications in schizophreniaMolecular Psychiatry, 2003
- Identification of Epilepsy Genes in Human and MouseAnnual Review of Genetics, 2001
- Molecular diagnosis in a child with sudden infant death syndromeThe Lancet, 2001
- Ion channels and epilepsyAmerican Journal of Medical Genetics, 2001
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- A Dominant Negative Isoform of the Long QT Syndrome 1 Gene ProductPublished by Elsevier ,1998
- Mutations in the hminK gene cause long QT syndrome and suppress lKs functionNature Genetics, 1997
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndromeNature Genetics, 1995
- Benign familial neonatal convulsions linked to genetic markers on chromosome 20Nature, 1989