The A1659V variant in SCN2A exhibits complex functional effects on channel activity, contributing to the clinical variability in related encephalopathies.
These results revealed the multifaceted functional effect of A1659V variant on channel activity and highlighted the complex genotype-phenotype correlation underlying significant clinical and pharmacological variability in SCN2A-related encephalopathies.
Corradi et al. (Sun,) studied this question.