以上来源于: WordNet
These findings hint at what happened to FOXP2 in our ancestors.
这些发现都在暗示我们祖先身上FOXP2基因所发生的变化。
Those researchers identified a mutation in FOXP2 as the cause of the dyspraxia.
学者确定FOXP2的突变是这种障碍的原因。
The most famous of these is FOXP2, damage to which prevents speech in modern humans.
最有名的当数FOXP2,这基因是与人类语言及言说障碍有关的基因。
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