The worldwide molecular spectrum and distribution of thalassaemia: a systematic review

Context Thalassaemia is one of the most common inherited autosomal recessive disorders around the world. A considerable amount of literature has been published about the type of mutations and the prevalence of thalassaemia, but findings are often contradictory. Objective This systematic review aimed...

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Hlavní autoři:	Mina Ebrahimi, Javad Mohammadi-Asl, Fakher Rahim
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Taylor & Francis Group 2021-05-01
Edice:	Annals of Human Biology
Témata:	co-inheritance α-thalassaemia β-thalassaemia mutations
On-line přístup:	http://dx.doi.org/10.1080/03014460.2021.1909135
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