A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2021-03-01 | PMID 33578253
Calame Daniel G, Houck Kimberly, Lotze Timothy and 2 more
