Voltage-dependent T-type calcium channel subunit alpha-1H
Definition:
References:
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[1]. Sarah E Heron, et al. Genetic variation of CACNA1H in idiopathic generalized epilepsy. Ann Neurol. 2004 Apr;55(4):595-6. [Content Brief]
[2]. Georgios Daniil, et al. CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism. EBioMedicine. 2016 Nov;13:225-236. [Content Brief]
[3]. M E Williams, et al. Structure and functional characterization of a novel human low-voltage activated calcium channel. J Neurochem. 1999 Feb;72(2):791-9. [Content Brief]
[4]. Veit-Simon Eckle, et al. Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility. J Physiol. 2014 Feb 15;592(4):795-809. [Content Brief]
[5]. L L Cribbs, et al. Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family. Circ Res. 1998 Jul 13;83(1):103-9. [Content Brief]
[6]. Yuriy Rzhepetskyy, et al. A Cav3.2/Stac1 molecular complex controls T-type channel expression at the plasma membrane. Channels (Austin). 2016 Sep 2;10(5):346-354. [Content Brief]
[7]. Ute I Scholl, et al. Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism. Elife. 2015 Apr 24;4:e06315. [Content Brief]
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