M Goulon, R Escourolle, A Barois, S Grosbuis. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Atrophy/congenitalAtrophy/geneticsAtrophy/pathologyCerebellar Ataxia/geneticsCerebellar Diseases/complicationsCerebellar Diseases/congenitalCerebellar Diseases/geneticsCerebellar Diseases/pathologyChild, PreschoolFemaleHumansInfantInfant, NewbornIntellectual Disability/etiologyMale
Year: 1968 PMID: 5686203
Source DB: PubMed Journal: Presse Med ISSN: 0032-7867 Impact factor: 1.228