Molecular basis and diagnosis of thalassemia
Blood Research
;
: S39-S43, 2021.
Article
Dans Anglais
| WPRIM
| ID: wpr-889648
ABSTRACT
Thalassemia is characterized by the impaired synthesis of globin chains due to disease-causing variants in α- or β-globin genes. In this review, we provide an overview of the molecular basis underlying α- and β-thalassemia, and of the current technologies used to characterize these disease-causing variants for the diagnosis of thalassemia.Understanding these molecular basis and technologies will prove to be beneficial for the accurate diagnosis of thalassemia.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
langue:
Anglais
Texte intégral:
Blood Research
Année:
2021
Type:
Article
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