强直性营养不良
失智症
肌萎缩侧索硬化
生物
遗传学
共济失调
突变
医学
基因
痴呆
疾病
病理
神经科学
作者
Sheng Chen,Zhi‐Ying Wu
出处
期刊:PubMed
日期:2014-11-01
卷期号:36 (11): 1145-51
摘要
Dynamic mutation diseases are genetic diseases caused by unstable repeat expansions in coding region or noncoding region. The unstable repeat expansions located in the noncoding region usually perform as large expansions which the standard PCR assay is difficult to amplify. Traditional detection methods, including Southern blot, are supposed to be time-consuming and labor-wasting. A new method called fluorescent repeat-primed PCR assay was brought into genetic diagnosis. Here, we reviewed the advances in repeat-primed PCR assay for the genetic diagnoses of myotonic dystrophy, Friedreich's ataxia, SCA10, and amyotrophic lateral sclerosis or frontotemporal dementia caused by C9 or f72 mutations.
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