Timothy Yu sent shockwaves through the genetic therapy world four years ago after revealing that he had developed — in under a year — a treatment tailored to a young girl’s unique genetic mutation.
That drug, dubbed Milasen in honor of the girl Mila, raised the bar on how truly personalized a medicine could be, and ignited efforts to develop the so-called n-of-1 therapies for more patients. Yet there was one question that kept nagging at Yu: How many others like Mila were out there?
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