Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3

F. Sangiuolo, E. Bruscia, F. Capon, S. Servidei, B. Dallapiccola, G. Novelli

Research output: Contribution to journalArticlepeer-review

Abstract

We previously mapped a distinctive autosomal dominant vacuolar neuromyopathy on human chromosome 19p13 in an 8 cM 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.

Original languageEnglish
Pages (from-to)809-812
Number of pages4
JournalEuropean Journal of Human Genetics
Volume8
Issue number10
DOIs
Publication statusPublished - 2000

Keywords

  • Chromosome 19
  • Linkage
  • Microsatellite markers
  • Vacuolar neuromyopathy

ASJC Scopus subject areas

  • Genetics(clinical)

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