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MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups.
Fanconi anemia (FA) consists of a group of at least five autosomal recessive disorders that share both clinical (e.g., birth defects and hematopoietic failure) and cellular (e.g., sensitivity to cross-linking agents and predisposition to apoptosis) features with each other. However, a common pathoge...
Gespeichert in:
| Veröffentlicht in: | J Clin Invest |
|---|---|
| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Society for Clinical Investigation
1997
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508494/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9389754/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119836 |
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