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0522971 - ÚOCHB 2021 RIV GB eng J - Journal Article
Stringer, Robin Nicholas - Jurkovicova-Tarabova, B. - Huang, S. - Haji-Ghassemi, O. - Idoux, R. - Liashenko, A. - Souza, I. A. - Rzhepetskyy, Yuriy - Lacinová, L. - Van Petegem, F. - Zamponi, G. W. - Pamphlett, R. - Weiss, Norbert
A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.
Molecular Brain. Roč. 13, Mar 6 (2020), č. článku 33. E-ISSN 1756-6606
Institutional support: RVO:61388963
Keywords : ALS * amyotrophic lateral sclerosis * motor neuron disease * CACNA1H * mutation * calcium channel * Cav3.2 channel * T-type channel * biophysics
OECD category: Biochemistry and molecular biology
Impact factor: 4.041, year: 2020
Method of publishing: Open access
https://molecularbrain.biomedcentral.com/articles/10.1186/s13041-020-00577-6#citeas
Permanent Link: http://hdl.handle.net/11104/0307384