Breakthrough CRISPR Therapy Gives New Hope to Baby With Rare Genetic Disorder
In a groundbreaking medical development, a baby in the United States known as "KJ" has become one of the first people in the world to be treated with a personalised CRISPR gene-editing therapy for a rare and often fatal genetic condition. KJ was diagnosed shortly after birth with carbamoyl-phosphate synthetase 1...
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