Could CRISPR Edit Out Every Genetic Disease by 2050?
Picture a hospital in 2050 where a diagnosis of a genetic disease prompts a single, precise edit – then a life resumes its ordinary rhythm. That future feels tantalizingly close after the first wave of CRISPR-based therapies proved one-time treatments can work in people. Yet every step forward reveals new knots: complex genetics, hard-to-reach organs, ...
