GENETIC SCREENING FOR G6PD MEDITERRANEAN MUTATION IN SOME •EGYPTIAN CHILDREN WITH G6PD DEFICIENCY
Hala Mohammed El-Nabeel El-Sayed;
Abstract
G6PD deficiency is the most wide spread red cell enzymopathy, affecting approximately 400 million people widespread.
This study was conducted on 21 G6PD deficient-patients, 17 males and 4 females, selected from the Haematology Clinic, New Children's Hospital, Cairo University.
In addition to routine laboratory investigations, all cases were subjected to quantitative G6PD enzyme assay, isoenzyme analysis by electrophoresis and PCR amplification using restriction endonuclease cleavage.
This study was conducted on 21 G6PD deficient-patients, 17 males and 4 females, selected from the Haematology Clinic, New Children's Hospital, Cairo University.
In addition to routine laboratory investigations, all cases were subjected to quantitative G6PD enzyme assay, isoenzyme analysis by electrophoresis and PCR amplification using restriction endonuclease cleavage.
Other data
| Title | GENETIC SCREENING FOR G6PD MEDITERRANEAN MUTATION IN SOME •EGYPTIAN CHILDREN WITH G6PD DEFICIENCY | Other Titles | مسح جينى لطفرة جين البحر الابيض المتوسط لانزيم (نازع الهيدروجين من الجلوكوز سداسى الفوسفات ) فى عينة من الاطفال المصريين المصابين بأنيميا الفول | Authors | Hala Mohammed El-Nabeel El-Sayed | Issue Date | 2000 |
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