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Increased Microerythrocyte Count in Homozygous α(+)-Thalassaemia Contributes to Protection against Severe Malarial Anaemia
BACKGROUND: The heritable haemoglobinopathy α(+)-thalassaemia is caused by the reduced synthesis of α-globin chains that form part of normal adult haemoglobin (Hb). Individuals homozygous for α(+)-thalassaemia have microcytosis and an increased erythrocyte count. α(+)-Thalassaemia homozygosity confe...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2267813/ https://ncbi.nlm.nih.gov/pubmed/18351796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pmed.0050056 |
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