Friday, November 15, 2024
HomeSehatanFDA menyetujui terapi gen pertama untuk penyakit sel sabit

FDA menyetujui terapi gen pertama untuk penyakit sel sabit



Watch CBS News



The Food and Drug Administration on Friday approved the first-ever gene-editing therapy that uses a cutting-edge technology called CRISPR to treat sickle cell disease. Dr. Jon LaPook has more.

Be the first to know

Get browser notifications for breaking news, live events, and exclusive reporting.




Source link

RELATED ARTICLES

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Most Popular

Recent Comments