A rare CACNA1H variant associated with amyotrophic lateral...

Molecular Brain 2020 / 12 Vol. 13; Iss. 1

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

Stringer, Robin N., Jurkovicova-Tarabova, Bohumila, Huang, Sun, Haji-Ghassemi, Omid, Idoux, Romane, Liashenko, Anna, Souza, Ivana A., Rzhepetskyy, Yuriy, Lacinova, Lubica, Van Petegem, Filip, Zamponi,
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Volume:
13
Journal:
Molecular Brain
DOI:
10.1186/s13041-020-00577-6
Date:
December, 2020
File:
PDF, 2.31 MB
2020
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