Direct genetic correction as a new method for diagnosis and molecular characterization of MHC class II deficiency
Published inMolecular therapy, vol. 6, no. 6, p. 824-829
Publication date2002
Abstract
Keywords
- Amino Acid Sequence
- Base Sequence
- Cell Line
- DNA-Binding Proteins/ genetics/metabolism
- Female
- Gene Therapy
- Genetic Complementation Test
- Genetic Vectors/genetics
- Histocompatibility Antigens Class II/ analysis/genetics
- Humans
- Immunologic Deficiency Syndromes/classification/ diagnosis/ genetics/pathology
- Lentivirus/genetics
- Male
- Molecular Sequence Data
- Nuclear Proteins
- Reproducibility of Results
- T-Lymphocytes/metabolism
- Trans-Activators/ genetics/metabolism
- Transcription Factors/ genetics/metabolism
- Transduction, Genetic
Affiliation Not a UNIGE publication
Research group
Citation (ISO format)
MATHEUX, Franck et al. Direct genetic correction as a new method for diagnosis and molecular characterization of MHC class II deficiency. In: Molecular therapy, 2002, vol. 6, n° 6, p. 824–829. doi: 10.1006/mthe.2002.0804
Main files (1)
Article
Identifiers
- PID : unige:11450
- DOI : 10.1006/mthe.2002.0804
- PMID : 12498778
ISSN of the journal1525-0016