The frequency of 6 beta-thalassemia mutations in the Iraqi patients from Najaf province
الباحث الأول:
Furqan Muein Auda
الباحثين الآخرين:
Afrodet A.Saleh Dawood Salman Ali
المجلة:
Gene Reports
تاريخ النشر:
None
مختصر البحث:
Thalassemia is the most common genetic disease in the province of Najaf in Iraq, where these patients suffer from deficiency or loss of the globin chains which leads to anemia and other complications. The study aimed to define the types of mutation …
Thalassemia is the most common genetic disease in the province of Najaf in Iraq, where these patients suffer from deficiency or loss of the globin chains which leads to anemia and other complications. The study aimed to define the types of mutation among patients with β-thalassemia major registered at the thalassemia unit in Al-Zahraa Teaching Hospital in AL-Najaf province. Blood samples were collected from 100 known patients with β-TM (51 males and 49 females), their ages about 3–18 year. The amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) technique was used for molecular diagnosis of six types of β-thalassemia mutations which are: -88 (C>T), codon 15 (G>A), IVS-1-5 (G>C), 8-9 (+G), 30 (G>C) and 8 (del-AA).
