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Edited by Alfred L. George, Jr., this collection examines disorders associated with variants in SCN2A, the gene encoding the neuronal sodium channel NaV1.2. Contributions connect the channel’s role in nerve-cell activity with the varied clinical features observed in affected individuals.
The book brings together perspectives on genetics, epilepsy, developmental conditions, functional mechanisms, pharmacology, and emerging treatment research. Patient, family, and foundation perspectives accompany the scientific chapters. Written for a professional and scholarly readership, the complete edition retains its contributor list, figures, references, and original publication notices.
Alfred L. George, Jr. (editor). SCN2A-Related Disorders. Cambridge University Press, 2024. https://doi.org/10.1017/9781009530361. CC BY-NC 4.0. Original edition unchanged.