A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity

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SYSNO	0522971
Title	A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity
Author(s)	Stringer, Robin Nicholas (UOCHB-X) [270/27] Jurkovicova-Tarabova, B. (SK) Huang, S. (CA) Haji-Ghassemi, O. (CA) Idoux, R. (CZ) Liashenko, A. (CZ) Souza, I. A. (CA) Rzhepetskyy, Yuriy (UOCHB-X) [270/27] Lacinová, L. (SK) Van Petegem, F. (CA) Zamponi, G. W. (CA) Pamphlett, R. (AU) Weiss, Norbert (UOCHB-X) [270/27]_{ORCID, RID}
Corespondence/senior	Weiss, Norbert - Korespondující autor
Source Title	Molecular Brain. Roč. 13, Mar 6 (2020). - : BioMed Central
Article number	33
Document Type	Článek v odborném periodiku
Institutional support	UOCHB-X - RVO:61388963
Language	eng
Country	GB
Keywords	ALS * amyotrophic lateral sclerosis * motor neuron disease * CACNA1H * mutation * calcium channel * Cav3.2 channel * T-type channel * biophysics
Cooperating institutions	Univerzita Karlova v Praze (Czech Republic)
URL	https://molecularbrain.biomedcentral.com/articles/10.1186/s13041-020-00577-6#citeas
Permanent Link	http://hdl.handle.net/11104/0307384

Number of the records: 1