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首页> 外文期刊>Neuromuscular disorders: NMD >Best practice guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies.
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Best practice guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies.

机译:杜兴/贝克肌营养不良症分子诊断的最佳实践指南。

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A meeting of 29 senior scientists from Europe, the USA, India and Australia, was held in Naarden, The Netherlands on November 14-16, 2008, to establish consensus Best Practice Guidelines for molecular diagnosis of Duchenne and Becker muscular dystrophy (DMD/BMD). New therapeutic trials for DMD demand accurate diagnosis of the disorder, especially where the therapy is targeted towards specific mutations. These guidelines aim to help diagnostic laboratories attain that accuracy by describing the minimum standards for acceptable molecular diagnostic testing of DMD. For the different types of clinical referral received by a molecular diagnostic laboratory, the guidelines recommend the appropriate tests to be carried out, interpretation of the results and how those results should be reported.
机译:2008年11月14日至16日,来自欧洲,美国,印度和澳大利亚的29位高级科学家会议在荷兰的纳尔登举行,以建立共识的杜兴氏和贝克尔肌营养不良症(DMD / BMD)分子诊断最佳实践指南。 )。针对DMD的新疗法试验要求对该疾病进行准确诊断,尤其是在针对特定突变的疗法中。这些准则旨在通过描述DMD可接受的分子诊断测试的最低标准来帮助诊断实验室达到该精度。对于分子诊断实验室接受的不同类型的临床转诊,指南建议进行适当的测试,结果的解释以及应如何报告这些结果。

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