Associated Papers
Identifying mutation hotspots reveals pathogenetic mechanisms of KCNQ2 epileptic encephalopathy.
Zhang J et al.
Scientific Reports, 2020
32179837 (PubMed )
Supplement: 41598_2020_61697_MOESM2_ESM.pdf
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
Grinton BE et al.
Epilepsia, 2015
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