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Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia (SCA) is the most severe form, while SC hemoglobinopathy (HbSC) is thought to be milder. Thus, we investigated the clinical manifestations and...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6988974/ https://ncbi.nlm.nih.gov/pubmed/31995624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0228399 |
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