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.
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Sangiuolo, F., Bruscia, E., Capon, F. et al. Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3. Eur J Hum Genet 8, 809–812 (2000). https://doi.org/10.1038/sj.ejhg.5200547
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DOI: https://doi.org/10.1038/sj.ejhg.5200547
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