Molecular Analysis of HS-111 and 3`HS1 Variations in β-Thalassemia Intermedia Patients with High Levels of HbF

Molecular Analysis of HS-111 and 3`HS1 Variations in β-Thalassemia Intermedia Patients with High Levels of HbF

Objective: To study the possible association between high levels of fetal haemoglobin(HbF) in β-thalassemia intermedia patients and HS-111 and 3`HS1 sequence variations.Materials and Methods: In this study, the 3' HS-1 and HS-111 regions of 30 ß-thalassaemiaintermedia patients (ß°/ß°) with high...

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Bibliographic Details
Main Authors: Mohammad Hamid, Morteza Karimipoor, Sirous Zeinali, Mohammad taghi Akbari, Leila Kokabi, Frouzandeh Mahjoubi
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2010-01-01
Series:Cell Journal
Subjects:
β-Thalassemia
Fetal Haemoglobin
Single-Strand Confirmation Polymorphism
Online Access:http://www.celljournal.org/library/upload/article/Hamid.pdf

Internet

http://www.celljournal.org/library/upload/article/Hamid.pdf

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