Style de citation APA (7e éd.)

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.

Style de citation Chicago (17e éd.)

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.

Style de citation MLA (8e éd.)

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.