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Myotonic Dystrophy and Congenital form: genetic and epigenetic marks associated with CTG/CAG repeat instability

Myotonic Dystrophy and Congenital form: genetic and epigenetic marks associated with CTG/CAG repeat instability
强直性肌营养不良和先天性形式：与 CTG/CAG 重复不稳定相关的遗传和表观遗传标记
批准号：
351792
负责人：
Pearson Christopher E
金额：
$7.29万
依托单位：
Hospital for Sick Children (Toronto)
依托单位国家：
加拿大
项目类别：
Operating Grants
财政年份：
2016
资助国家：
加拿大
项目状态：
已结题
起止时间：
2016-04-01 至 2017-04-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=351792&lang=en
关键词：
Congenital Myotonic Dystrophy Dna Methylation Epigenetics Myotonic Dystrophy Type 1 Parent-Of-Origin Effect Repeat Instability

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中文摘要
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英文摘要
40 human diseases, including Myotonic Dystrophy (DM), are inherited in a manner that the symptoms become more evident through family generations. These diseases are caused by mutations in repeated DNAs. If one considers a gene as though it were a sentence
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