Episodic ataxia results from voltage-dependent potassium channels with altered functions
- 1 December 1995
- Vol. 15 (6), 1449-1454
- https://doi.org/10.1016/0896-6273(95)90022-5
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1Nature Genetics, 1994
- Evidence that the S6 segment of the Shaker voltage-gated K+ channel comprises part of the poreNature, 1994
- The S4–S5 loop contributes to the ion-selective pore of potassium channelsNeuron, 1993
- Deletion analysis of K+ channel assemblyNeuron, 1993
- The internal quaternary ammonium receptor site of Shaker potassium channelsNeuron, 1993
- Calcium-activated potassium channels expressed from cloned complementary DNAsNeuron, 1992
- Putative receptor for the cytoplasmic inactivation gate in the Shaker K+ channelNature, 1991
- Autosomal dominant episodic ataxia: A heterogeneous syndromeMovement Disorders, 1986
- A dominantly inherited syndrome with continuous motor neuron dischargesAnnals of Neurology, 1983
- THE SYNDROME OF CONTINUOUS MUSCLE FIBER ACTIVITYActa Neurologica Scandinavica, 1977