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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2021.4
- 수록면
- 39 - 43 (5page)
- DOI
- 10.5045/br.2021.2020332
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초록· 키워드
오류제보하기
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.
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