Molecular basis of a-thalassaemia
<p>a-thalassaemias is an autosomal recessive disorder, in which there is impaired production of the a-globin chains of haemoglobin. It is associated with microcytic hypochromic anaemia, and a clinical phenotype varying from almost asymptomatic to a lethal haemolytic anaemia. It is probably the...
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| Format: | Article |
| Language: | English |
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PAGEPress Publications
2011-12-01
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| Series: | Thalassemia Reports |
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| Online Access: | http://www.pagepressjournals.org/index.php/thal/article/view/303 |