S Refsum, H Skre. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Ataxia/epidemiologyAtaxia/geneticsAtrophyBrain Diseases/geneticsCerebellar Ataxia/epidemiologyCerebellar Ataxia/geneticsCharcot-Marie-Tooth Disease/geneticsFriedreich Ataxia/geneticsGenes, DominantGenes, RecessiveHumansMuscle Spasticity/geneticsNorwayParaplegia/geneticsSyndrome
Year: 1978 PMID: 369332
Source DB: PubMed Journal: Adv Neurol ISSN: 0091-3952