Article Details

AAV Vectors in Gene Therapy: Overcoming Barriers for Muscular Dystrophy Treatment

Retrieved on: 2024-10-28 19:07:18

Tags for this article:

Click the tags to see associated articles and topics

AAV Vectors in Gene Therapy: Overcoming Barriers for Muscular Dystrophy Treatment. View article details on hiswai:

Excerpt

Where we need improvement is in AAVs that target specific cell types, like muscle stem cells for CRISPR therapies. If you can target and edit muscle ...

Article found on: www.neurologylive.com

View Original Article

This article is found inside other hiswai user's workspaces. To start your own collection, sign up for free.

Sign Up