C J de Weerdt, L N Went. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultCentral Nervous System Diseases/complicationsConsanguinityFemaleGenotypeHumansMaleMental Disorders/complicationsMiddle AgedMultiple Sclerosis/complicationsNeurologic ManifestationsOptic Atrophy/complicationsOptic Atrophy/diagnosisOptic Atrophy/geneticsParaplegia/complicationsPedigreeReflex, AbnormalScotomaSex Chromosomes
Year: 1971 PMID: 5139723 DOI: 10.1111/j.1600-0404.1971.tb07507.x
Source DB: PubMed Journal: Acta Neurol Scand ISSN: 0001-6314 Impact factor: 3.209