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: | Charoenkwan P., Taweephon R., Sae-Tung R., Thanarattanakorn P., Sanguansermsri T. |
---|---|
Format: | Article |
Language: | English |
Published: |
2014
|
Online Access: | http://www.scopus.com/inward/record.url?eid=2-s2.0-18844409532&partnerID=40&md5=71784ca68f91eb65199d54c8e968d5cd http://www.ncbi.nlm.nih.gov/pubmed/15921165 http://cmuir.cmu.ac.th/handle/6653943832/1914 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
Language: | English |
Similar Items
-
Molecular and clinical features of Hb H disease in northern Thailand
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) -
Clinical features and molecular analysis in Thai patients with HbH disease
by: Vichai Laosombat, et al.
Published: (2018) -
Detection of Hb H disease genotypes common in Northern Thailand by quantitative real-time polymerase chain reaction and high resolution melting analyses
by: Seeratanachot T., et al.
Published: (2014) -
Detection of Hb H disease genotypes common in Northern Thailand by quantitative real-time polymerase chain reaction and high resolution melting analyses
by: Teerapat Seeratanachot, et al.
Published: (2018)