Počet záznamů: 1
A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity
- 1.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
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 4.041, rok: 2020
Způsob publikování: Open access
https://molecularbrain.biomedcentral.com/articles/10.1186/s13041-020-00577-6#citeas
http://hdl.handle.net/11104/0307384
Počet záznamů: 1