Fanconi anemia: A paradigm of the Molecular detection of common mutations in Egyptian Fanconi anemia patients
Rehab Mostafa Mohamed Mosaad;
Abstract
Introduction: FA-A is the most frequent complementation group representing approximately two-thirds of the FA patients in the majority of countries. Aim of the work: screening the most common mutations in exons 27, 34, 38 and 43 of FANCA gene in the Egypt
Other data
| Title | Fanconi anemia: A paradigm of the Molecular detection of common mutations in Egyptian Fanconi anemia patients | Other Titles | أنيميا الفانكونى : مثال لأكتشاف الطفرات الجينية الأكثر انتشارا فى مرضى أنيميا الفانكونى المصريين | Authors | Rehab Mostafa Mohamed Mosaad | Keywords | Fanconi anemia: A paradigm of the Molecular detection of common mutations in Egyptian Fanconi anemia patients | Issue Date | 2013 | Description | Introduction: FA-A is the most frequent complementation group representing approximately two-thirds of the FA patients in the majority of countries. Aim of the work: screening the most common mutations in exons 27, 34, 38 and 43 of FANCA gene in the Egypt |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 115076G1764.pdf | 89.62 kB | Adobe PDF | View/Open |
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