Cap +1 mutation; an unsuspected cause of beta thalassaemia transmission in Pakistan
Objective: Thalassemia is one of the most common genetic disorders worldwide. Cap +1 mutation which causes ‘silent beta thalassemia’ is present around all ethnic groups of Pakistan. This study was designed to detect the frequency of Cap+1 mutation in Pakistani Population.Materials and Methods: Molec...
Main Authors: | Sadia Usman Babar, Moinuddin Moinuddin, Muhammad Usman Abdul Karim |
---|---|
Format: | Article |
Language: | English |
Published: |
Galenos Publishing House
2009-12-01
|
Series: | Turkish Journal of Hematology |
Subjects: | |
Online Access: | http://www.journalagent.com/z4/download_fulltext.asp?pdir=tjh&plng=eng&un=TJH-25338 |
Similar Items
-
Common Β- Thalassaemia Mutations in
by: P Azarfam, et al.
Published: (2005-01-01) -
Common Β- Thalassaemia Mutations in Northwestern Iran
by: MA Hossainpour-Faizi, et al.
Published: (2005-01-01) -
HBB Gene Mutations and Their Pathological Impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia
by: Hanan Kamel M. Saad, et al.
Published: (2023-03-01) -
The “Thal-index” with the BTT prediction.exe to discriminate Beta thalassaemia traits from other microcytic anaemias.
by: Nilanga Nishad
Published: (2014-08-01) -
Haemoglobin E/Beta Thalassaemia- A Study in BSMMU
by: Md Abdul Aziz, et al.
Published: (2010-04-01)