Ion Channel Mutations and Diseases of Skeletal Muscle
Open Access
- 31 December 1997
- journal article
- review article
- Published by Elsevier in Neurobiology of Disease
- Vol. 4 (3-4) , 254-264
- https://doi.org/10.1006/nbdi.1997.0158
Abstract
No abstract availableKeywords
This publication has 71 references indexed in Scilit:
- Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker.The Journal of general physiology, 1996
- Electrophysiological properties of the hypokalaemic periodic paralysis mutation (R528H) of the skeletal muscle α1S subunit as expressed in mouse L cellsFEBS Letters, 1996
- Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel α-subunit gene (SCN5A) to band 3p21Cytogenetic and Genome Research, 1995
- Voltage-dependent regulation of modal gating in the rat SkM1 sodium channel expressed in Xenopus oocytes.The Journal of general physiology, 1994
- Molecular physiology of anion channelsCurrent Opinion in Cell Biology, 1994
- A calcium channel mutation causing hypokalemic periodic paralysisHuman Molecular Genetics, 1994
- Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletionHuman Molecular Genetics, 1994
- Sodium channel mutations in paramyotonia congenita uncouple inactivation from activationNeuron, 1994
- Structure and Modulation of Na+ and Ca2+ ChannelsAnnals of the New York Academy of Sciences, 1993
- MYOTONIA IN THE GOAT *Annals of the New York Academy of Sciences, 1979