Molecular and clinical features of Hb H disease in northern Thailand
Clinical assessment, hematological studies and molecular analyses were performed in 102 pediatric patients with Hb H disease in northern Thailand. A total of six mutations of the α-globin gene, which produced five genotypes, were detected. All patients had an α0-thalassemia (thal) deletion on one ch...
Saved in:
Main Authors: | Pimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, Pattra Thanarattanakorn, Torpong Sanguansermsri |
---|---|
Format: | Journal |
Published: |
2018
|
Subjects: | |
Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=18844409532&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62105 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
Similar Items
-
Molecular and clinical features of Hb H disease in northern Thailand
by: Charoenkwan P., et al.
Published: (2014) -
Hemoglobin E levels in double heterozygotes of hemoglobin E and sea-type α-thalassemia
by: Pimlak Charoenkwan, et al.
Published: (2018) -
Clinical features and molecular analysis in Thai patients with HbH disease
by: Vichai Laosombat, et al.
Published: (2018) -
Cord blood screening for Α-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: Correlation with genotypes and hematologic parameters
by: Pimlak Charoenkwan, et al.
Published: (2018) -
Hematological and molecular characterization of beta-thalassemia/HB Tak compound heterozygote
by: Charoenkwan P., et al.
Published: (2014)