A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy.
Lauritano A, Moutton S, Longobardi E, Tran Mau-Them F, Laudati G, Nappi P, Soldovieri MV, Ambrosino P, Cataldi M, Jouan T, Lehalle D, Maurey H, Philippe C, Miceli F, Vitobello A, Taglialatela M.
Lauritano A, et al. Among authors: taglialatela m.
Epilepsia Open. 2019 Aug 11;4(3):464-475. doi: 10.1002/epi4.12353. eCollection 2019 Sep.
Epilepsia Open. 2019.
PMID: 31440727
Free PMC article.