Researchers Kiran Musunuru (L) and Rebecca Ahrens-Nicklas (Photo credit: Ryan Collerd)
The inside story of the six-month sprint to create the first custom CRISPR therapy for one infant’s rare disease
PHILADELPHIA — Soon after Kyle Patrick Muldoon, Jr. was born in August 2024, his doctors knew something was wrong. KJ, as …
Sign up to read this article for free.
Get free access to a limited number of articles, plus choose newsletters to get straight to your inbox.
