Lentiviral Hematopoietic Stem and Progenitor Cell Gene Therapy for Wiskott-Aldrich Syndrome (WAS): Up to 8 Years of Follow up in 17 Subjects Treated Since 2010

Title
Lentiviral Hematopoietic Stem and Progenitor Cell Gene Therapy for Wiskott-Aldrich Syndrome (WAS): Up to 8 Years of Follow up in 17 Subjects Treated Since 2010
Authors
Keywords
-
Journal
BLOOD
Volume 134, Issue Supplement_1, Pages 3346-3346
Publisher
American Society of Hematology
Online
2019-11-14
DOI
10.1182/blood-2019-124665

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