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Molecular basis and diagnosis of thalassemia
Blood Research ; : S39-S43, 2021.
Article in En | WPRIM | ID: wpr-897352
Responsible library: WPRO
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.
Full text: 1 Index: WPRIM Type of study: Diagnostic_studies Language: En Journal: Blood Research Year: 2021 Type: Article
Full text: 1 Index: WPRIM Type of study: Diagnostic_studies Language: En Journal: Blood Research Year: 2021 Type: Article