Description of Hb Évora (
Hb Évora
hemoglobinopathy
red blood cell (RBC)
thalassemia
Journal
Hemoglobin
ISSN: 1532-432X
Titre abrégé: Hemoglobin
Pays: England
ID NLM: 7705865
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
pubmed:
5
2
2022
medline:
20
5
2022
entrez:
4
2
2022
Statut:
ppublish
Résumé
α-Thalassemia (α-thal) is caused by DNA deletions or point mutations in the genes coding for the α-globin chains and can lead to hemolytic anemia in its carriers. If only one of the four α genes is affected, the mutation is mostly discovered by chance, as the carriers are asymptomatic. Hb Évora (
Identifiants
pubmed: 35114882
doi: 10.1080/03630269.2022.2034643
doi:
Substances chimiques
Hemoglobins, Abnormal
0
alpha-Globins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM