Characterisation of a new alpha thalassemia 1 defect due to a partial deletion of the alpha globin gene complex.

A new deletion causing alpha thalassemia has been characterised in a Greek family. Detailed mapping of the alpha gene complex shows that the deletion extends for 5.2 kb and removes the whole of the alpha 2 gene and the 5' end of the alpha 1 gene. The affected chromosome, therefore produces no normal...

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Pubblicato in:	Nucleic Acids Res
Autori principali:	Pressley, L, Higgs, D R, Aldridge, B, Metaxatou-Mavromati, A, Clegg, J B, Weatherall, D J
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Oxford University Press 1980
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC324266/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6255436/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/8.21.4889
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