Selected Reading
- Anderson WF: Prospects for Human Gene Therapy. Science 226:401, 1984
- Blaese RM: Development of gene therapy for immunodeficiency: Adenosine deaminase deficiency. Pediatr Res 33 (1 Suppl): S49, 1993
- Culver K et al: Lymphocytes as cellular vehicles for gene therapy in mouse and man. Proc Natl Acad Sci(USA) 88:3155, 1991
- Kantoff PW et al: Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer. Proc Natl Acad Sci(USA) 83:6563, 1986
- Kohn DB et al: Gene therapy for neonates with ADA-deficient SCID by retroviral-mediated transfer of the human ADA cDNA into umbilical cord CD34+ cells. J Cell Biochem Suppl 18A: 238, 1994
- Nienhuis AW, McDonagh KT, Bodine DM: Gene transfer Into hematopoietic stem cells. Cancer 67 (10 Suppl): 2700, 1991
- Wijnaendts L et al: Development of immunologic functions after bone marrow transplantation In 33 patients with severe combined immunodeficiency. Blood 74:2212, 1989