意大利一项合作研究在DMD和BMD患者中检测到528个基因内缺失。

F Mioni, G A Danieli, A Cao, M Cau, S Colonna-Romano, A E Covone, P De Leonardis, R De Leo, M G Esposito, L Felicetti
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引用次数: 0

摘要

报告了一项合作研究的结果,该研究涉及居住在意大利领土上的大约三分之一的DMD和BMD病例。通过内含子分析断点频率发现DMD患者区域组之间存在显著差异(撒丁岛的内含子2、11和50,意大利东北部的内含子9和45),而BMD患者区域组之间没有观察到区域差异。这些差异涉及意大利相同的地区,以前的研究通过不同的标记进行,确定为“遗传分化”。这些数据支持了一些内含子序列在种群之间差异分布的可能性,促进了肌营养不良蛋白基因中缺失断点的起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study.

The results of a collaborative study involving about one third of the total DMD and BMD cases living in the Italian territory are reported. The analysis of the breakpoint frequency by intron revealed significant differences among regional groups of DMD patients (for introns 2, 11 and 50 in Sardinia and for introns 9 and 45 in northeastern Italy), whereas no regional differences were observed among regional groups of BMD patients. These differences involve the same Italian regions which previous studies, performed by different markers, identified as "genetically differentiated". The data support the possibility of a differential distribution among populations of some intronic sequences, facilitating the origin of deletion breakpoints within the dystrophin gene.

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