Friday, May 24, 2019

FDA approves innovative gene therapy to treat pediatric patients with spinal muscular atrophy, a rare disease and leading genetic cause of infant mortality - FDA Press Releases

FDA approves innovative gene therapy to treat pediatric patients with spinal muscular atrophy, a rare disease and leading genetic cause of infant mortality

from FDA Press Releases RSS Feed http://bit.ly/2VQSFE5
via IFTTT

No comments:

Post a Comment