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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. Dostupné z: doi: 10.1186/s13041-020-00577-6.
Počet záznamů: 1