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 |
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Pages (from-to) | 809-812 |
Number of pages | 4 |
Journal | European Journal of Human Genetics |
Volume | 8 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2000 |
Keywords
- Chromosome 19
- Linkage
- Microsatellite markers
- Vacuolar neuromyopathy
ASJC Scopus subject areas
- Genetics(clinical)