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Mitochondrial Changes in β(0)-Thalassemia/Hb E Disease
The compound β°-thalassemia/Hb E hemoglobinopathy is characterized by an unusually large range of presentation from essentially asymptomatic to a severe transfusion dependent state. While a number of factors are known that moderate presentation, these factors do not account for the full spectrum of...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4836671/ https://ncbi.nlm.nih.gov/pubmed/27092778 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153831 |
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