目前，MBL的结构-功能关系未明，MBL基因突变引起调理吞噬缺损的机制不清，这些均需进一步研究予以阐明。
However, the relationship between structure and functions of MBL and the mechanisms by which MBL structure gene mutations cause opsonic deficiency are to be clarified.
研究者们希望，通过对该基因突变和相关蛋白结构的深入了解可以开发出有效的药物治疗来抑制突变基因的激活。
The researchers hope that understanding more about the gene's mutations and the structure of the protein may lead to drug treatments to help ensure that mutant copies of the gene are inactive.
研究者们希望，通过对该基因突变和相关蛋白结构的深入了解可以开发出有效的药物治疗来抑制突变基因的激活。
The researchers hope that understanding more about the gene's mutations and the structure of the protein may lead to drug treatments to help ensure that mutant copies of the gene are inactive.
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