Laura B. Jones, Colin H. Peters, Richard E. Rosch, Richard E. Rosch, Maxine Owers, Elaine Hughes, . . . Peter C. Ruben. (2021). The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A..
Chicago Style (17th ed.) CitationLaura B. Jones, et al. The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A., 2021.
MLA (9th ed.) CitationLaura B. Jones, et al. The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function. Frontiers Media S.A., 2021.
Warning: These citations may not always be 100% accurate.