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Two point mutations are responsible for G6PD polymorphism in Sardinia.

The human X-linked gene encoding glucose 6-phosphate dehydrogenase (G6PD) is highly polymorphic; more than 300 G6PD variants have been identified. G6PD deficiency in different geographical areas appears to have arisen through independent mutational events, but within the same population it may also...

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Detalhes bibliográficos
Main Authors: De Vita, G, Alcalay, M, Sampietro, M, Cappelini, M D, Fiorelli, G, Toniolo, D
Formato: Artigo
Idioma:Inglês
Publicado em: 1989
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715414/
https://ncbi.nlm.nih.gov/pubmed/2912069
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