Associated Papers
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
Asadollahi R et al.
Human Molecular Genetics, 2023
Sodium channelopathies of skeletal muscle and brain.
Mantegazza M et al.
Physiological Reviews, 2021
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes.
Begemann A et al.
Molecular Medicine (cambridge, Mass.), 2019
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