Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions
- 1 September 2004
- journal article
- review article
- Published by Springer Nature in Genetica
- Vol. 122 (1) , 37-45
- https://doi.org/10.1007/s10709-004-1441-9
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- SCNM1, a Putative RNA Splicing Factor That Modifies Disease Severity in MiceScience, 2003
- High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spotGenomics, 2003
- Sodium channel Na v 1.6 is localized at nodes of Ranvier, dendrites, and synapsesProceedings of the National Academy of Sciences, 2000
- Reduced spontaneous activity in the dorsal cochlear nucleus of Scn8a mutant miceBrain Research, 1999
- Functional Analysis of a Voltage‐Gated Sodium Channel and Its Splice Variant from Rat Dorsal Root GangliaJournal of Neurochemistry, 1998
- Phenotype variation and newcomers in ion channel disordersHuman Molecular Genetics, 1997
- Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’Nature Genetics, 1995
- Potassium channel blockers and impulse propagation in murine motor endplate diseaseMuscle & Nerve, 1987
- A CEREBELLAR ABNORMALITY IN THE MOUSE WITH MOTOR END‐PLATE DISEASENeuropathology and Applied Neurobiology, 1985
- Electrophysiological and morphological studies of a motor nerve in ‘motor endplate disease’ of the mouseProceedings of the Royal Society of London. B. Biological Sciences, 1982