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- Title
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.
- Authors
Sangiuolo, F; Bruscia, E; Capon, F; Servidei, S; Dallapiccola, B; Novelli, G
- Abstract
We previously mapped a distinctive autosomal dominant vacuolar neuromyopathy on human chromosome 19p13 in an 8cM region, delimited by D19S209 and D19S177 markers. We now report the fine mapping of the disease locus within an interval of 250 Kb by haplotype analysis performed using a set of 11 novel microsatellite markers isolated from the candidate region.
- Publication
European journal of human genetics : EJHG, 2000, Vol 8, Issue 10, p809
- ISSN
1018-4813
- Publication type
Journal Article
- DOI
10.1038/sj.ejhg.5200547