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31. Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1. (3rd April 2015)

32. Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study. (20th October 2016)

34. The phenotype of SCN8A developmental and epileptic encephalopathy. (18th September 2018)