Lentiviral Vectors with Cellular Promoters Correct Anemia and Lethal Bone Marrow Failure in a Mouse Model for Diamond-Blackfan Anemia. (2017)

First Author: Debnath S
Attributed to:  Development of a lentiviral vector for gene therapy of ADA deficiency funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ymthe.2017.04.002

PubMed Identifier: 28434866

Publication URI: http://europepmc.org/abstract/MED/28434866

Type: Journal Article/Review

Volume: 25

Parent Publication: Molecular therapy : the journal of the American Society of Gene Therapy

Issue: 8

ISSN: 1525-0016