Get all your news in one place.
100's of premium titles.
One app.
Start reading
The Conversation
The Conversation
John Bergeron, Emeritus Robert Reford Professor and Professor of Medicine, McGill University

Solving the puzzle of cystic fibrosis and its treatments is a Nobel Prize-worthy breakthrough

The discovery of the cystic fibrosis gene led to treatments and long-term survival for patients. (Shutterstock)

The nomination deadline to recognize transformative discoveries for the Nobel prize in physiology or medicine is fast approaching. These nominations are by invitation only and are due by the end of January.

Besides those for the lifesaving COVID-19 vaccines, several others are prominent. This includes the discovery of the cystic fibrosis gene and the drugs to treat the disease. The disease was first identified in 1938, and is no longer a cause of near-certain deaths in infants. Today, Canada leads the world with a 52-year median age of survival for patients with cystic fibrosis.

Sign up to read this article
Read news from 100's of titles, curated specifically for you.
Already a member? Sign in here
Related Stories
Top stories on inkl right now
One subscription that gives you access to news from hundreds of sites
Already a member? Sign in here
Our Picks
Fourteen days free
Download the app
One app. One membership.
100+ trusted global sources.