Human Genome Project may help find treatment for muscular dystrophy
Professor Kay Davies is head of the Department of Human Anatomy and Human Genetics at the University of Oxford. One of the disorders her group is studying is Duchenne muscular dystrophy (DMD), one of 20 different types of muscular dystrophy. The dystrophin gene is located on the X chromosome, which is present in duplicate in women and as a single copy in men. This means that boys who inherit the disease will do so from a mother who carries one copy of the defective gene.