Artwork

Content provided by podcast@nature.com and Springer Nature Limited. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by podcast@nature.com and Springer Nature Limited or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Player FM - Podcast App
Go offline with the Player FM app!

Audio long read: Hope, despair and CRISPR — the race to save one woman’s life

23:04
 
Share
 

Manage episode 430852818 series 2509444
Content provided by podcast@nature.com and Springer Nature Limited. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by podcast@nature.com and Springer Nature Limited or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

In India, a group of researchers raced to develop a CRISPR-based genome editing therapy to save the life of a young woman with a rare neurodegenerative disease. Despite a valiant effort, the pace of research was ultimately too slow to save her life. While many are convinced that these therapies could offer hope to those with overlooked genetic conditions, it will likely take years to develop the techniques needed to quickly create bespoke treatments, something people in need don't have.


This is an audio version of our Feature: Hope, despair and CRISPR — the race to save one woman’s life



Hosted on Acast. See acast.com/privacy for more information.

  continue reading

736 episodes

Artwork
iconShare
 
Manage episode 430852818 series 2509444
Content provided by podcast@nature.com and Springer Nature Limited. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by podcast@nature.com and Springer Nature Limited or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

In India, a group of researchers raced to develop a CRISPR-based genome editing therapy to save the life of a young woman with a rare neurodegenerative disease. Despite a valiant effort, the pace of research was ultimately too slow to save her life. While many are convinced that these therapies could offer hope to those with overlooked genetic conditions, it will likely take years to develop the techniques needed to quickly create bespoke treatments, something people in need don't have.


This is an audio version of our Feature: Hope, despair and CRISPR — the race to save one woman’s life



Hosted on Acast. See acast.com/privacy for more information.

  continue reading

736 episodes

All episodes

×
 
Loading …

Welcome to Player FM!

Player FM is scanning the web for high-quality podcasts for you to enjoy right now. It's the best podcast app and works on Android, iPhone, and the web. Signup to sync subscriptions across devices.

 

Quick Reference Guide