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 SizeFormat
115076G1764.pdf89.62 kBAdobe PDFView/Open
Recommend this item

Similar Items from Core Recommender Database

Google ScholarTM

Check

views 5 in Shams Scholar
downloads 3 in Shams Scholar


Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.