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
Citation
F. Sangiuolo et al., Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3, EUR J HUM G, 8(10), 2000, pp. 809-812
Citations number
6
Categorie Soggetti
Molecular Biology & Genetics
Journal title
EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN journal
10184813 → ACNP
Volume
8
Issue
10
Year of publication
2000
Pages
809 - 812
Database
ISI
SICI code
1018-4813(200010)8:10<809:FMOADA>2.0.ZU;2-8
Abstract
We previously mapped a distinctive autosomal dominant vacuolar neuromyopath y on human chromosome 19p13 in an 8 cM region, delimited by D19S209 and D19 S177 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.