Alpha-thalassaemia.
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hypochromic anaemia, and a clinical phenotype varying from almost asymptomatic to a lethal haemolytic anaemia.It is probably the most common monogenic gene disorder in the world and is especially frequen...
| Main Authors: | , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2010
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