DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

References

Lauritano A, Moutton S, Longobardi E. et al.
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy.

Epilepsia Open 2019;
4 (03) 464-475

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