APA (7th ed.) Citation

Stringer, R. N., Jurkovicova-Tarabova, B., Huang, S., Haji-Ghassemi, O., Idoux, R., Liashenko, A., . . . Weiss, N. (2020). A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity. Molecular Brain, 13(1), 1. https://doi.org/10.1186/s13041-020-00577-6

Chicago Style (17th ed.) Citation

Stringer, Robin N., et al. "A Rare CACNA1H Variant Associated with Amyotrophic Lateral Sclerosis Causes Complete Loss of Cav3.2 T-type Channel Activity." Molecular Brain 13, no. 1 (2020): 1. https://doi.org/10.1186/s13041-020-00577-6.

MLA (9th ed.) Citation

Stringer, Robin N., et al. "A Rare CACNA1H Variant Associated with Amyotrophic Lateral Sclerosis Causes Complete Loss of Cav3.2 T-type Channel Activity." Molecular Brain, vol. 13, no. 1, 2020, p. 1, https://doi.org/10.1186/s13041-020-00577-6.