Molecular Characterization of Cosenza Mutation among Patients with Glucose-6-Phosphate Dehydrogenase Deficiency in huzestan Province, Southwest Iran

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. It is also characterized by remarkable molecular and biochemical heterogeneity. According to previous investigations...

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Detalles Bibliográficos
Autores principales: Kazemi Nezhad, Seyed Reza, Fahmi, Fatemeh, Khatami, Saeid Reza, Musaviun, Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2011
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558731/
https://www.ncbi.nlm.nih.gov/pubmed/23365477

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558731/
https://www.ncbi.nlm.nih.gov/pubmed/23365477

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