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Stanford Maternal and Child Health Research Institute
Cystic Fibrosis as a Paradigm for Precision Medicine
Well into the 21st century, Cystic Fibrosis remains the most common life-shortening inherited disease and in the United States, 1,000 children are born with the disease every year. A consequence of mutations in the Cystic Fibrosis Trans-membrane Conductance Regulator (CFTR) gene, remarkable clinical and scientific efforts have led to fast-paced improvements in the treatment of Cystic Fibrosis. Drs. Milla and Sellers will review the progress towards a cure for cystic fibrosis and how this is informed by in-depth genetic knowledge at the individual level.

Jun 1, 2020 12:00 PM in Pacific Time (US and Canada)

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