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Thalassemic hemoglobinopathies.

Hemoglobinopathies are due to changes in the normal amino acid sequence of globin. Thalassemias result from imbalance in the normal coordinated synthesis of the globin subunits that make up the hemoglobin tetramer. It is now apparent that a single globin gene can have coding region mutations which s...

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Detalles Bibliográficos
Main Authors: Steinberg, M. H., Adams, J. G.
Formato: Artigo
Idioma:Inglês
Publicado: 1983
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1916350/
https://ncbi.nlm.nih.gov/pubmed/6359893
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