The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity
<p>Abstract</p> <p>Background</p> <p>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 o...
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Format: | Book |
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BMC,
2010-02-01T00:00:00Z.
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A1234.567 |
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