Neuroferritinopathy in a French family with late onset dominant dystonia - Chinnery, P F; Curtis, A R J; Fey, C; Coulthard, A; Crompton, D; Curtis, A; Lombés, A; Burn, J (Journal of medical genetics, 2003)
Keywords: Adult; Age of Onset; Ataxia; basal ganglia; Basal Ganglia Diseases - genetics; Basal Ganglia Diseases - pathology; Basal Ganglia Diseases - physiopathology; Corpus Striatum - pathology; dystonia; Dystonia - genetics; Dystonia - pathology; Dystonia - physiopathology; England; France; Genes; Genes, Dominant - genetics; Genomes; Haplotypes; Haplotypes - genetics; Humans; Iron - metabolism; Middle Aged; movement disorder; Mutation; neuroferritinopathy; Online Mutation Report; Patients; Polypeptides; England; France; United Kingdom--UK