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A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity
- 1.Stringer, R. N., Jurkovicova-Tarabova, B., Huang, S., Haji-Ghassemi, O., Idoux, R., Liashenko, A., Souza, I. A., Rzhepetskyy, Y., Lacinová, L., Van Petegem, F., Zamponi, G. W., Pamphlett, R., Weiss, N. A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity. Molecular Brain. 2020, 13(Mar 6), 33. E-ISSN 1756-6606. Available: doi: 10.1186/s13041-020-00577-6.
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