Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants

G6PD deficiency is a monogenic, X-linked genetic defect with a worldwide prevalence of around 400 million people and an overall prevalence of 8.5% in India. Hemolytic anemia is encountered in only a small proportion of patients with G6PD variants and is usually triggered by some exogenous agent. Alt...

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Опубликовано в: :Indian J Hematol Blood Transfus
Главные авторы: Arunachalam, Arun Kumar, Sumithra, S., Maddali, Madhavi, Fouzia, N. A., Abraham, Aby, George, Biju, Edison, Eunice S.
Формат: Artigo
Язык:Inglês
Опубликовано: Springer India 2019
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Original Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7229042/
https://ncbi.nlm.nih.gov/pubmed/32425388
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-019-01205-7
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