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Cystic Fibrosis: From Gene to Precision Medicines 2020
April 2, 2020 @ 6:00 pm - 7:30 pm
Cystic Fibrosis: From Gene to Precision Medicines 2020
Public Lecture by Professor David Sheppard
In the inherited disease cystic fibrosis (CF), thick sticky mucus blocks the lungs and bowel, leading to breathing difficulties and problems digesting food. Thirty years ago, the faulty gene responsible for CF was identified. This lecture will highlight research that has led to the development of precision medicines that target the root cause of disease, which are transforming the treatment of CF.
School Of Physiology, Pharmacology & Neuroscience
Organiser of Cystic Fibrosis: From Gene to Precision Medicines
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