These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits. McKeown L; Robinson P; Jones OT Acta Pharmacol Sin; 2006 Jul; 27(7):799-812. PubMed ID: 16787562 [TBL] [Abstract][Full Text] [Related]
4. Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels. Striessnig J; Bolz HJ; Koschak A Pflugers Arch; 2010 Jul; 460(2):361-74. PubMed ID: 20213496 [TBL] [Abstract][Full Text] [Related]
5. [Calcium channels and human genetic diseases]. Zhang YH; Wu XR Zhonghua Er Ke Za Zhi; 2004 Jul; 42(7):547-50. PubMed ID: 15324581 [No Abstract] [Full Text] [Related]
6. Calcium channels and channelopathies of the central nervous system. Pietrobon D Mol Neurobiol; 2002 Feb; 25(1):31-50. PubMed ID: 11890456 [TBL] [Abstract][Full Text] [Related]
7. Hallmarks of the channelopathies associated with L-type calcium channels: a focus on the Timothy mutations in Ca(v)1.2 channels. Bidaud I; Lory P Biochimie; 2011 Dec; 93(12):2080-6. PubMed ID: 21664226 [TBL] [Abstract][Full Text] [Related]
8. The role of ion-regulatory membrane proteins of excitation-contraction coupling and relaxation in inherited muscle diseases. Froemming GR; Ohlendieck K Front Biosci; 2001 Jan; 6():D65-74. PubMed ID: 11145921 [TBL] [Abstract][Full Text] [Related]