Gene Therapy and Bone Marrow Transplants for Sickle Cell Disease
Jul 20, 2018•33 min•Season 1Ep. 4
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Episode description
In this episode of Breaking Through, Madeline speaks with Children’s Hospital of Philadelphia (CHOP) researchers Stefano Rivella, PhD, and William Peranteau, MD, about gene therapy and fetal bone marrow transplants to cure sickle cell disease. She also talks about how CHOP’s Daisy Days fundraising campaign is fueling their research.
To find out how you can help make tomorrow’s breakthroughs at CHOP, click here.
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