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The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity
BACKGROUND: The clinical syndrome of thalassemia intermedia (TI) results from the β-globin genotypes in combination with factors to produce fetal haemoglobin (HbF) and/or co-inheritance of α-thalassemia. However, very little is currently known of the molecular basis of Chinese TI patients. METHODS:...
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Main Authors: | , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2010
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2845123/ https://ncbi.nlm.nih.gov/pubmed/20181291 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-31 |
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