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News-Medical.Net on MSNPersonalized gene editing corrects fatal infant metabolic disorder in world-first treatmentResearchers have used a personalised base-editing gene therapy to successfully treat an infant with carbamoyl-phosphate ...
After 3 doses of tailor-made treatment, an infant with a rare, life-threatening urea cycle disorder is thriving ...
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MedPage Today on MSNIn a First, CRISPR Used to Treat Infant With Ultra-Rare DiseaseA tailored CRISPR base-editing therapy was given for the first time to an infant who was born with a rare genetic disease, with promising effects, researchers reported.
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