APA (7th ed.) Citation

RN, S., B, J., S, H., O, H., R, I., A, L., . . . N, W. (2020). A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity. Molecular brain, 13(1), 33. https://doi.org/10.1186/s13041-020-00577-6

Chicago Style (17th ed.) Citation

RN, Stringer, 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): 33. https://doi.org/10.1186/s13041-020-00577-6.

MLA (9th ed.) Citation

RN, Stringer, 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. 33, https://doi.org/10.1186/s13041-020-00577-6.