Current developments in the design of onco-retrovirus and lentivirus vector systems for hematopoietic cell gene therapy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference193 articles.
1. Correction of ADA-SCID by Stem Cell Gene Therapy Combined with Nonmyeloablative Conditioning
2. Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease
3. Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy
4. A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency
5. T Lymphocyte-Directed Gene Therapy for ADA − SCID: Initial Trial Results After 4 Years
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