Sign Up to like & get
recommendations!
0
Published in 2020 at "Hemoglobin"
DOI: 10.1080/03630269.2020.1768109
Abstract: Abstract Hb Westmead (α122(H5)His>Gln) (HBA2: c.369C>G) is a common α-globin variant causing α-thalassemia (α-thal) in Mainland China. In this study, we report the hematological characteristics in Hb Westmead carriers in a Chinese population. There were…
read more here.
Keywords:
hematological characteristics;
thal;
compound heterozygotes;
hba2 369c ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2020 at "Hemoglobin"
DOI: 10.1080/03630269.2020.1793774
Abstract: Abstract The −50 (G>A) (HBB: c.-100G>A) mutation was first reported as a β-thalassemia (β-thal) allele in a Chinese family. However, the hematological features of carriers with this variant are not available. In this study, we…
read more here.
Keywords:
hematological characteristics;
thal;
globin gene;
hbb 100g ... See more keywords