Non-deletional alpha thalassaemia: a review | Orphanet Journal of Rare Diseases | Full Text

Non-deletional alpha thalassaemia: a review | Orphanet Journal of Rare Diseases | Full Text

Non-deletional alpha thalassaemia: a review

Defective synthesis of the α-globin chain due to mutations in the alpha-globin genes and/or its regulatory elements leads to alpha thalassaemia syndrome. Complete deletion of the 4 alpha-globin genes results i...

Authors:Ibrahim Kalle Kwaifa, Mei I. Lai and Sabariah Md Noor

Citation:Orphanet Journal of Rare Diseases 2020 15:166

Content type:Review

 

Published on: 29 June 2020

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