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alpha-Thalassaemia in Apulia: biosynthetic studies.

Analysis of haemoglobin chain synthesis was performed in 15 Apulian patients with Hb H disease and in their patients and offspring. The Apulian carriers of Hb H disease show a marked imbalance of alpha and beta chain synthesis (0.39 +/- 0.1) with variable clinical and haematological manifestations....

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Detalhes bibliográficos
Main Authors: Guanti, G, Lonoce, A, Pietrapertosa, A, Polimeno, G, Tannoia, N
Formato: Artigo
Idioma:Inglês
Publicado em: 1983
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049047/
https://ncbi.nlm.nih.gov/pubmed/6876112
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