Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation
与ATP1A3突变相关的家族性儿童期起病进行性小脑综合征
期刊:Neurology-Genetics
影响因子:3.7
doi:10.1212/NXG.0000000000000145
Jaffer, Fatima; Fawcett, Katherine; Sims, David; Heger, Andreas; Houlden, Henry; Hanna, Michael G; Kingston, Helen; Sisodiya, Sanjay M
