单基因疾病
网络释义专业释义
一种单基因遗传疾病 monogenic disease
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single gene disorder - 引用次数：1 参考来源 - 定量联结人抗凝血酶Ⅲ的变异及其临床表现 Quantitative Coupling of Human Antithrombin Ⅲ Mutations with Their Clinical Outcomes
·2,447,543篇论文数据，部分数据来源于NoteExpress
双语例句原声例句
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针对这种明确的单基因疾病有可能开展基因治疗。
It is possible to cure the patients with XLSA by gene therapy because it is a single gene disorder.
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但是，单基因疾病研究能从新的方面揭示基因组生物学。
But study of monogenic diseases can reveal new aspects of genomic biology.
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GPCR的突变及基因多态性将引发各种疾病，目前已经发现有30多种单基因疾病与此相关。
Mutant GPCR and genetic variation will cause diseases and responsible for more than 30 different human diseases which have been identified to date.
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Usually this is a disease that's caused by a defect in a single gene.
通常在疾病是由,单基因缺陷引起时才可行
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