What Next: TBD

Maria Simulescu

Episode Notes Last May, a 12-year-old with sickle cell anemia was the first person to receive a new gene therapy to treat the disease. The process is painful, expensive, and still frightening and uncertain, but biomedical researchers are cautiously calling it a “cure.” Guests: Gina Kolata, medical reporter for the New York Times Deb and Keith Cromer, parents to Kendric Cromer, the first person in the world to go through a commercially approved gene therapy for sickle cell anemia. Want more What

What Next: TBD https://slate.com/ - 24.11.2024 10:00

din zilele anterioare

What Next: TBD https://slate.com/ - 24.11.2024 10:00