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Summary Expression Phenotypes Gene Literature (72) GO Terms (15) Nucleotides (226) Proteins (51) Interactants (141) Wiki
XB--977294

Papers associated with cav2 (and Disease Ontology)



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Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia., Stendel C, D'Adamo MC, Wiessner M, Dusl M, Cenciarini M, Belia S, Nematian-Ardestani E, Bauer P, Senderek J, Klopstock T, Pessia M., Int J Mol Sci. May 27, 2020; 21 (11):             

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2., Jeng CJ, Chen YT, Chen YW, Tang CY., Am J Physiol Cell Physiol. April 1, 2006; 290 (4): C1209-20.

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects., Müllner C, Broos LA, van den Maagdenberg AM, Striessnig J., J Biol Chem. December 10, 2004; 279 (50): 51844-50.

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