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Neonatal hemolytic anemia does not always indicate thalassemia: a case report
BACKGROUND: Congenital erythropoietic porphyria is a rare autosomal recessive disorder that affects heme-porphyrin synthesis. This disorder is due to the genetic defect of uroporphyrinogen III cosynthase. This defect results in the accumulation of high amounts of uroporphyrin I in all tissues, leadi...
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| Publicado no: | BMC Res Notes |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5596485/ https://ncbi.nlm.nih.gov/pubmed/28899405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-017-2803-6 |
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