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A Case of Diamond Blackfan Anemia (DBA) with Mutation in Ribosomal Protein S19
Diamond Blackfan Anemia (DBA) is a rare disorder which presents with anemia in early infancy. This disorder is genetically and clinically heterogeneous in nature. The inheritance is mainly autosomal dominant. Approximately 25% of the cases are associated with craniofacial anomalies and some cases ma...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
JCDR Research and Publications (P) Limited
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3939545/ https://ncbi.nlm.nih.gov/pubmed/24596764 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2014/7018.3899 |
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