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Scientists give pioneering gene therapy to infant patient
美国科学家为婴儿实施个性化基因疗法

Child suffering from rare liver disease shows improved health after treatment
患有罕见肝病的儿童在治疗后健康状况有所改善。
Doctors Kiran Musunuru, left, and Rebecca Ahrens-Nicklas hold the baby who received the Crispr gene editing technology

Scientists in the US have performed the first personalised gene therapy on a child with a life-threatening rare disease, raising the prospect of similar bespoke treatments for many other disorders.

美国科学家首次为一名患有危及生命的罕见疾病的儿童实施了个性化基因疗法,这为许多其他疾病的定制化治疗带来了希望。

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