Chen J D, Denton M J, Morgan G, Pearn J H, Mackinlay A G
Division of Pathology, Prince of Wales Hospital, Randwick, NSW, Australia.
Am J Hum Genet. 1988 May;42(5):777-80.
Deletion is a common cause of Duchenne muscular dystrophy (DMD). Field-inversion gel electrophoresis, in conjunction with Southern blot hybridization, was used to detect large SfiI DNA fragments in the DMD locus. Two unrelated boys with DMD were found to have abnormal sized DNA fragments resulting from deletions. Some of the female relatives of these patients were also shown by this method to have deletions in the DMD locus.
缺失是杜兴氏肌营养不良症(DMD)的常见病因。场反转凝胶电泳结合Southern印迹杂交技术,用于检测DMD基因座中的大型SfiI DNA片段。发现两名患有DMD的无关男孩存在因缺失导致的异常大小的DNA片段。通过该方法还显示,这些患者的一些女性亲属在DMD基因座中也存在缺失。