a-Thalassemia trait caused by frameshift mutations in exon 2 of the a2-globin gene: HBA2:c.131delT and HBA2:c.143delA
We describe two frameshift mutations associated with an a-thalassemia (a-thal) phenotype, identified in three unrelated individuals investigated for persistent microcytosis. The first mutation, HBA2:c.131delT, is located in codon 43, and the second, HBA2:c.143delA, is located in codon 47. Both are d...
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Bibliographic Details
| Main Authors: |
Finlayson, J.,
Ghassemifar, Reza,
Holmes, P.,
Grey, D.,
Newbound, C.,
Pell, N.,
Jennens, M.,
Greenwood, L.,
Beilby, J. |
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| Format: | Journal Article
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| Published: |
2012
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| Online Access: | http://hdl.handle.net/20.500.11937/47879
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