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Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon.

A Brazilian family of Italian descent is described in which the beta-thalassaemia gene is interacting with an alpha chain variant Hb Hasharon (alpha 47 Asp leads to His). One patient who was affected by homozygous beta 0-thalassaemia and heterozygous alpha Hasharon displayed the clinical picture of...

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Hlavní autoři: Zago, M A, Costa, F F, Bottura, C
Médium: Artigo
Jazyk:Inglês
Vydáno: 1982
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048957/
https://ncbi.nlm.nih.gov/pubmed/7154040
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