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Clinical Manifestations of α-Thalassemia

α-Thalassemia mutations affect up to 5% of the world’s population. The clinical spectrum ranges from an asymptomatic condition to a fatal in utero disease. Hemoglobin H disease results from mutations of three α-globin genes. Deletional forms result in a relatively mild anemia, whereas nondeletional...

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Detalhes bibliográficos
Autor principal: Vichinsky, Elliott P.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3633183/
https://ncbi.nlm.nih.gov/pubmed/23543077
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a011742
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