Cita APA (7a ed.)

Jones, L. B., Peters, C. H., Rosch, R. E., Rosch, R. E., Owers, M., Hughes, E., . . . Ruben, P. C. (2021). The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A.

Cita Chicago Style (17a ed.)

Jones, Laura B., et al. The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A, 2021.

Cita MLA (8a ed.)

Jones, Laura B., et al. The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A, 2021.