Article
Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.
Human genetics - 1 May 1993
Lunkes A, Gispert S, Enczmann J, Auburger G
Abstract excerpt
This study addresses the question whether the different forms of autosomal dominant cerebellar ataxia (ADCA) are related to different ethnic/geographical regions in Europe. One mutation in families originating from Holland, Prussia and Italy has previously been localized to chromosome 6p (SCA1 locus), whereas the mutation in families of Iberic origin has been excluded from chromosome 6p. In a Danish...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
