外显子
杜氏肌营养不良
遗传学
肌营养不良
基因
医学
多重聚合酶链反应
人口
肌营养不良蛋白
生物
分子生物学
聚合酶链反应
环境卫生
作者
G. Narsinga Rao,Tajamul Hussain,Nisha Devi,Suman Jain,Giriraj R Chandak,Mithun Raj
出处
期刊:PubMed
日期:2003-01-01
卷期号:57 (1): 1-6
被引量:10
摘要
66 unrelated patients from Southern India with Duchenne Muscular Dystrophy (DMD) were studied for intragenic deletion in 18 exons and Pm region of the DMD gene using multiplex PCR. Of these 41 (62.1%) showed intragenic deletions. 78% of the deletions were located at the distal hotspot region (44-55 exons) and 22% of the deletions were located at the proximal region (exon 2-19). Exon 50 is most frequently deleted. Deletions in isolated cases were significantly more compared to familial cases. The lower incidence reported from South India compared to North India, is suggestive of variations in the Southern and Northern population.
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