Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) disease
A rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has α-thal-1 (- SEA type) together with a non productive Hb Queens Park (HBA1:c.98T > A) [α32(B13)Met→Lys] α1-globin variant. No abnormal hemoglobin (Hb) fraction was detected b...
Saved in:
Main Authors: | Suravee Sroymora, Sumalee Jindadamrongwech, Punnee Butthep, Suporn Chuncharunee |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/13709 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions
by: Suravee Sroymora, et al.
Published: (2018) -
Hb tak and Hb Q-Thailand in thai patients are S-window hemoglobin variants revealed by high performance liquid chromatography
by: Sumalee Jindadamrongwech, et al.
Published: (2018) -
Identification of HB anantharaj [α11(a9)LYS→GLU] AS HB j-uenchang-wuming [α11(a9)LYS→GLN]
by: J. Svasti, et al.
Published: (2018) -
Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A > T; beta 82(EF6)Lys -> Met] with Hb H Disease
by: Lee, Shir-Ying, et al.
Published: (2021) -
Hematological Analysis in Thai Samples with Deletional and Nondeletional HbH Diseases
by: Sakorn Pornprasert, et al.
Published: (2018)