Gene mutation and qualitative enzyme assay of G6PD enzyme deficiency in neonatal hyperbilirubinemia
Othman Rizk Abdel Meguid Mishref;
Abstract
Background: Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency variants is essential, especially since the biochemical characterization has lost its significance due to the individual variability. As a result, cases can be m
Other data
| Title | Gene mutation and qualitative enzyme assay of G6PD enzyme deficiency in neonatal hyperbilirubinemia | Other Titles | Gene mutation and qualitative enzyme assay of G6PD enzyme deficiency in neonatal hyperbilirubinemia | Authors | Othman Rizk Abdel Meguid Mishref | Keywords | Gene mutation and qualitative enzyme assay of G6PD enzyme deficiency in neonatal hyperbilirubinemia | Issue Date | 2013 | Description | Background: Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency variants is essential, especially since the biochemical characterization has lost its significance due to the individual variability. As a result, cases can be m |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 122113R9486.pdf | 768.32 kB | Adobe PDF | View/Open |
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