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

doi:10.1038/sj.ejhg.5200547

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 journal › Article › peer-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 language	English
Pages (from-to)	809-812
Number of pages	4
Journal	European Journal of Human Genetics
Volume	8
Issue number	10
DOIs	https://doi.org/10.1038/sj.ejhg.5200547
Publication status	Published - 2000

Keywords

Chromosome 19
Linkage
Microsatellite markers
Vacuolar neuromyopathy

ASJC Scopus subject areas

Genetics(clinical)

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10.1038/sj.ejhg.5200547

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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.",

keywords = "Chromosome 19, Linkage, Microsatellite markers, Vacuolar neuromyopathy",

author = "F. Sangiuolo and E. Bruscia and F. Capon and S. Servidei and B. Dallapiccola and G. Novelli",

year = "2000",

doi = "10.1038/sj.ejhg.5200547",

language = "English",

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AU - Sangiuolo, F.

AU - Bruscia, E.

AU - Capon, F.

AU - Servidei, S.

AU - Dallapiccola, B.

AU - Novelli, G.

PY - 2000

Y1 - 2000

N2 - 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.

AB - 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.

KW - Chromosome 19

KW - Linkage

KW - Microsatellite markers

KW - Vacuolar neuromyopathy

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

Abstract

Keywords

ASJC Scopus subject areas

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