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Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction

✍ Scribed by Satoshi Fujishita; Noritoshi Shibuya; Norio Niikawa; Shigenobu Nagataki

Publisher: Nature Publishing Group
Year: 1991
Tongue: English
Weight: 467 KB
Volume: 36
Category: Article
ISSN: 1435-232X
DOI: 10.1007/bf01883605

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## For the Focus Section on Array-CGH The dystrophinopathies, which include Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and X-linked dilated cardiomyopathy, are X-linked recessive neuromuscular disorders caused by mutations in the dystrophin gene (DMD). Approximately 70% of