Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat.
Chronic granulomatous disease (CGD) is a rare inherited condition rendering neutrophils incapable of killing invading pathogens. This condition is due to the failure of a multicomponent microbicidal oxidase that normally yields a low-midpoint-potential b cytochrome (cytochrome b245). Although defect...
Gespeichert in:
| Veröffentlicht in: | Proc Natl Acad Sci U S A |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
1991
|
| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC51317/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2011585/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.7.2753 |
| Tags: |
Keine Tags, Fügen Sie das erste Tag hinzu!
|