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α-Thalassemia in the American Negro

In Italian and Chinese patients with the α-thalassemia syndromes the production of α-chain of normal hemoglobin is decreased relative to that of β-chain in reticulocytes. In this study the relative rates of α- and β-chain synthesis were determined in members of three Negro families with α-thalassemi...

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Detalhes bibliográficos
Main Authors: Schwartz, Elias, Atwater, Jean
Formato: Artigo
Idioma:Inglês
Publicado em: 1972
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC302140/
https://ncbi.nlm.nih.gov/pubmed/5061833
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