Update on gene therapy for hereditary hematological disorders
Author:
Publisher
Informa UK Limited
Subject
Cardiology and Cardiovascular Medicine,General Medicine,Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1586/14779072.1.2.215
Reference117 articles.
1. Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease
2. ••Describes cure of several pediatricpatients with severe immune deficiency byex vivogene transfer.
3. Gene therapy of severe combined immunodeficiencies
4. Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy
5. T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates
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