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Cystic Fibrosis as a Paradigm for Precision MedicineJun 01, 2020 (Mon) | 12:00 PM -1:00 AM
Webinar link will be sent after registration.
: This will be a virtual event. , CA
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. Register here: https://stanford.zoom.us/webinar/register/WN_IG-bDj53RU6GJ42KWFjPDw Department: Stanford Maternal and Child Health Research Institute Contact: Roxanna Van Norman | 6504985444 | roxannav@stanford.edu Presenter(s):
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