Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA<inf>2</inf> Levels on Capillary Electrophoresis

© 2017 Indian Society of Haematology & Transfusion Medicine A misdiagnosis of β-thalassemia carrier in samples with Hb Tak and HbD-Punjab, the β-variants, can be a cause of inappropriate genetic counseling thus having a new case of β-thalassemia major. A capillary electrophoresis (CE) is very...

Full description

Saved in:
Bibliographic Details
Main Authors: Panyasai S., Sakkhachornphop S., Pornprasert S.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85017103358&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40577
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University