Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus
doi: 10.1007/bf00206755
pmid: 2203673
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus
We have localised a dystrophin-related autosomal gene called DMDL (Duchenne muscular dystrophy-like) to human chromosome 61q24 by in situ hybridisation. Using restriction fragment length polymorphism analysis in two mouse species, we have localised the homologous gene Dmdl in the mouse to chromosome 10 proximal to the Myb oncogene. A neuromuscular disease locus dystrophia muscularis (dy) has previously been assigned to this region of mouse chromosome 10.
- Institut Pasteur France
- Northamptonshire Healthcare NHS Foundation Trust United Kingdom
- Oxford University Hospitals NHS Trust United Kingdom
- John Radcliffe Hospital United Kingdom
Male, Mice, Inbred BALB C, Genetic Linkage, Chromosome Mapping, Muscle Proteins, Mice, Inbred Strains, Muscular Dystrophy, Animal, Muscular Dystrophies, Dystrophin, Mice, Inbred C57BL, Mice, Animals, Humans, Chromosomes, Human, Pair 6
Male, Mice, Inbred BALB C, Genetic Linkage, Chromosome Mapping, Muscle Proteins, Mice, Inbred Strains, Muscular Dystrophy, Animal, Muscular Dystrophies, Dystrophin, Mice, Inbred C57BL, Mice, Animals, Humans, Chromosomes, Human, Pair 6
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