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

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Title: A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.
Authors: Stringer, Robin N.1,2 (AUTHOR), Jurkovicova-Tarabova, Bohumila3 (AUTHOR), Huang, Sun4 (AUTHOR), Haji-Ghassemi, Omid5 (AUTHOR), Idoux, Romane1 (AUTHOR), Liashenko, Anna1 (AUTHOR), Souza, Ivana A.4 (AUTHOR), Rzhepetskyy, Yuriy1 (AUTHOR), Lacinova, Lubica3 (AUTHOR), Van Petegem, Filip5 (AUTHOR), Zamponi, Gerald W.4 (AUTHOR), Pamphlett, Roger6 (AUTHOR), Weiss, Norbert1 (AUTHOR) weiss@uochb.cas.cz
Source: Molecular Brain. 3/6/2020, Vol. 13 Issue 1, p1-11. 11p.
Database: Academic Search Ultimate
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  Data: A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.
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  Data: <searchLink fieldCode="JN" term="%22Molecular+Brain%22">Molecular Brain</searchLink>. 3/6/2020, Vol. 13 Issue 1, p1-11. 11p.
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        Value: 10.1186/s13041-020-00577-6
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              Text: 3/6/2020
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