z-logo
open-access-imgOpen Access
Gene Therapy mediated by lentiviral vector transduced CD34+ cells for the treatment of Wiskott-Aldrich Syndrome
Author(s) -
Samantha Scaramuzza,
Francesca Ferrua,
Castiello Maria,
Stefania Giannelli,
Luca Biasco,
Fabio Ciceri,
Roncarolo Maria Grazia,
Anna Villa,
Naldini Luigi,
Aiuti Alessandro
Publication year - 2013
Publication title -
frontiers in immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 124
ISSN - 1664-3224
DOI - 10.3389/conf.fimmu.2013.02.00403
Subject(s) - genetic enhancement , wiskott–aldrich syndrome , viral vector , haematopoiesis , cd34 , clonogenic assay , progenitor cell , stem cell , bone marrow , immunology , medicine , biology , cancer research , virology , in vivo , gene , genetics , recombinant dna

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here