Calcium channelopathies
- 1 March 2000
- journal article
- review article
- Published by Elsevier in Kidney International
- Vol. 57 (3) , 794-802
- https://doi.org/10.1046/j.1523-1755.2000.00917.x
Abstract
No abstract availableKeywords
This publication has 60 references indexed in Scilit:
- Cloning and Expression of a Novel Member of the Low Voltage-Activated T-Type Calcium Channel FamilyJournal of Neuroscience, 1999
- Cloning and Characterization of α1H From Human Heart, a Member of the T-Type Ca 2+ Channel Gene FamilyCirculation Research, 1998
- An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessNature Genetics, 1998
- Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessNature Genetics, 1998
- Molecular characterization of a neuronal low-voltage-activated T-type calcium channelNature, 1998
- Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channelsJournal of Neuroscience, 1995
- Structure and Functional Expression of a Member of the Low Voltage-Activated Calcium Channel FamilyScience, 1993
- Primary structure and functional expression from complementary DNA of a brain calcium channelNature, 1991
- Rat brain expresses a heterogeneous family of calcium channels.Proceedings of the National Academy of Sciences, 1990
- Primary structure of the receptor for calcium channel blockers from skeletal muscleNature, 1987