G6PD gene polymorphisms in Egyptian deficient patients
Omnia Yahia Ibrahim Abd El Dayem;
Abstract
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy, affecting over 400 million people all over the world.
The G6PD gene, being located on the long arm of the X-chromosome, G6PD deficiency follows an X- linked p
The G6PD gene, being located on the long arm of the X-chromosome, G6PD deficiency follows an X- linked p
Other data
| Title | G6PD gene polymorphisms in Egyptian deficient patients | Other Titles | التحورات في الجين المسئول عن أنيميا الفول في المرضى المصريين | Authors | Omnia Yahia Ibrahim Abd El Dayem | Keywords | G6PD gene polymorphisms in Egyptian deficient patients | Issue Date | 2010 | Description | Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy, affecting over 400 million people all over the world. The G6PD gene, being located on the long arm of the X-chromosome, G6PD deficiency follows an X- linked p |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 96885r3154.pdf | 121.91 kB | Adobe PDF | View/Open |
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