Saturday, August 14, 2021
CRISPR/Cas9 gene-edited HSPCs for Friedreich’s ataxia
Stephanie Cherqui, PhD, University of California, San Diego, La Jolla, CA, describes a CRISPR/Cas9 gene-edited hematopoietic stem and progenitor cell (HSPC)-based therapy for Friedreich’s ataxia (FRDA)
Subscribe to:
Posts (Atom)