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Ribosomal Protein S24 Gene Is Mutated in Diamond-Blackfan Anemia
Diamond-Blackfan anemia (DBA) is a rare congenital red-cell aplasia characterized by anemia, bone-marrow erythroblastopenia, and congenital anomalies and is associated with heterozygous mutations in the ribosomal protein (RP) S19 gene (RPS19) in ∼25% of probands. We report identification of de novo...
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| Hoofdauteurs: | , , , , , , , , , , , , , , , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The American Society of Human Genetics
2006
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1698708/ https://ncbi.nlm.nih.gov/pubmed/17186470 |
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