Linkage of proximal myotonic myopathy to chromosome 3q
作者： K. Ricker , T. Grimm , M. C. Koch , C. Schneider , W. Kress
DOI: 10.1212/WNL.52.1.170
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摘要: Article abstract We performed genetic linkage analysis in nine German proximal myotonic myopathy (PROMM) families using DNA-markers D3S1541 and D3S1589 from the region of recently discovered gene locus dystrophy type 2 ( DM2 ) on chromosome 3q. Two-point supplied an lod score 5.9. conclude that a causing PROMM is located may be allelic disorders or caused by closely linked genes.
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