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Volumn 70, Issue 4, 2002, Pages 269-277

Spectrum of β-thalassemia mutations and their association with allelic sequence polymorphisms at the β-globin gene cluster in an Eastern Indian population

Author keywords

globin gene; thalassemia mutation; Allelic sequence polymorphisms; Hypersensitive site; Locus control region

Indexed keywords

BETA GLOBIN; CIS ACTING ELEMENT; DEOXYRIBONUCLEASE I;

EID: 0036328606     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.10117     Document Type: Article
Times cited : (38)

References (30)
  • 6
    • 0009877505 scopus 로고    scopus 로고
    • Full activity from human β-globin locus control region transgenes requires 5′HS1, distal β-globin promoter, and 3′ β-globin sequences
    • (1998) Blood , vol.82 , pp. 853-862
    • Pasceri, P.1    Pannell, D.2    Wu, X.3    Ellis, J.4
  • 7
    • 0030062162 scopus 로고    scopus 로고
    • Fetal hemoglobin in sickle cell anemia: Relation to regulatory sequences cis to the β-globin gene
    • (1996) Blood , vol.87 , pp. 1604-1611
    • Lu, Z.-H.1    Steinberg, M.H.2
  • 14
    • 0032055871 scopus 로고    scopus 로고
    • Hydrops fetalis caused by α-thalassemia: An emerging health care problem
    • (1998) Blood , vol.91 , pp. 2213-2222
    • Chui, D.H.K.1    Waye, J.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.