Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease.

Two mutations in the nicotinic acetylcholine receptor subunit A4 (CHRNA4) in a family with autosomal dominant sleep-related hypermotor epilepsy.

Cancer immune control needs senescence induction by interferon-dependent cell cycle regulator pathways in tumours

ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.