AI 导读
@BroadInstitute 的科学家们正在寻找不明罕见病病例的根本病因，但可能的突变列表极为庞大。 借助 Atlas，研究人员锁定了 DNM1 基因中的一个关键突变，并在实验室中得到确认和验证。https://t.co/OIsV3TCOuO
正文
Scientists at @BroadInstitute search for the underlying causes of unexplained rare disease cases, but the list of possible mutations is vast.
Using Atlas, researchers pinpointed a critical mutation in the DNM1 gene, which was confirmed and validated in the lab. https://t.co/OIsV3TCOuO
来源：@GoogleDeepMind · x.com