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Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation

机译:与遗传性宪法等异构的林奇综合征家庭MLH1启动子甲基化相关的遗传事件多样性

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摘要

Purpose: Constitutional epimutations are an alternative to genetic mutations in the etiology of genetic diseases. Some of these epimutations, termed secondary, correspond to the epigenetic effects of cis-acting genetic defects transmitted to the offspring following a Mendelian inheritance pattern. In Lynch syndrome, a few families with such apparently heritable MLH1 epimutations have been reported so far.
机译:目的:宪法缩醛是遗传疾病病因中遗传突变的替代品。 其中一些称为次要的缩影对应于在孟德尔遗传模式之后传播到后代的顺式作用遗传缺陷的表观遗传效应。 在林奇综合征中,迄今为止已经报道了一些具有如此明显遗传的MLH1缩影的家庭。

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