[PDF][PDF] A locus for autosomal dominant “pure” hereditary spastic paraplegia maps to chromosome 19q13

E Reid, AM Dearlove, O Osborn, MT Rogers… - The American Journal of …, 2000 - cell.com
E Reid, AM Dearlove, O Osborn, MT Rogers, DC Rubinsztein
The American Journal of Human Genetics, 2000cell.com
Genetic loci for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) have
been mapped to chromosomes 2p, 8q, 12q, 14q, and 15q. We undertook a genomewide
linkage screen of a large family with ADPHSP, for which linkage at all previously identified
ADPHSP loci was excluded. Analysis of markers on chromosome 19q gave a peak pairwise
LOD score of 3.72 at D19S420, allowing assignment of a novel ADPHSP locus (which we
have termed" SPG12") to this region. Haplotype construction and analysis of recombination …
Summary
Genetic loci for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) have been mapped to chromosomes 2p, 8q, 12q, 14q, and 15q. We undertook a genomewide linkage screen of a large family with ADPHSP, for which linkage at all previously identified ADPHSP loci was excluded. Analysis of markers on chromosome 19q gave a peak pairwise LOD score of 3.72 at D19S420, allowing assignment of a novel ADPHSP locus (which we have termed "SPG12") to this region. Haplotype construction and analysis of recombination events narrowed the SPG12 locus to a 16.1-cM region between markers D19S868 and D19S902.
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