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研究人员发明一种新方法,有助于确定变异在多发性硬化症中所发挥作用的程度,新成果发明在5月在线出版的《自然-结构与分子生物学》期刊上。通过人类基因组的研究,科学家们能够确定变异与特定疾病的关系,但他们至今仍难以将许多变异与某个特定的基因联系起来,从而导致了遗传学研究与疾病治疗的分离,但是,如果不能确定靶向基因,遗传性疾病是难以治疗的。
The researchers invented a new method to help determine the extent to which mutations play a role in multiple sclerosis. The new findings were published in the journal Nature - Structure and Molecular Biology published online in May. Through the study of the human genome, scientists can determine the relationship between mutations and specific diseases, but so far they still find it difficult to relate many mutations to a particular gene, resulting in the separation of genetic research from disease treatment. However, if they can not Identifying targeted genes, genetic diseases are difficult to treat.