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Volumn 77, Issue 4, 2004, Pages 384-386

Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background

Author keywords

Hemoglobin Titusville; Low oxygen affinity variant; Northern European background

Indexed keywords

ALPHA GLOBIN; ASPARAGINE; ASPARTIC ACID; GENOMIC DNA; HEMOGLOBIN TITUSVILLE; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

EID: 9644270584     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.20209     Document Type: Article
Times cited : (26)

References (7)
  • 1
    • 0034936469 scopus 로고    scopus 로고
    • Databases of human hemoglobin variants and other resources at the globin gene server
    • Hardison RC, Chui DHK, Riemer C, et al. Databases of human hemoglobin variants and other resources at the globin gene server (http://globin.cse.psu. edu/). Hemoglobin 2001;25:183-193.
    • (2001) Hemoglobin , vol.25 , pp. 183-193
    • Hardison, R.C.1    Chui, D.H.K.2    Riemer, C.3
  • 2
    • 0016857109 scopus 로고
    • Hemoglobin Titusville: α94 Asp replaced by Asn. A new hemoglobin with a lowered affinity for oxygen
    • Schneider RG, Atkins RJ, Hosty TS, et al. Hemoglobin Titusville: α94 Asp replaced by Asn. A new hemoglobin with a lowered affinity for oxygen. Biochim Biophys Acta 1975;400:365-373.
    • (1975) Biochim Biophys Acta , vol.400 , pp. 365-373
    • Schneider, R.G.1    Atkins, R.J.2    Hosty, T.S.3
  • 3
    • 0034778460 scopus 로고    scopus 로고
    • Hb H hydrops foetalis syndrome: A case report and review of literature
    • Lorey F, Charoenkwan P, Witkowska HE, et al. Hb H hydrops foetalis syndrome: a case report and review of literature. Br J Haematol 2001;115:72-78.
    • (2001) Br J Haematol , vol.115 , pp. 72-78
    • Lorey, F.1    Charoenkwan, P.2    Witkowska, H.E.3
  • 4
    • 0022808364 scopus 로고
    • Alpha-thalassemia in blacks: Genetic and clinical aspects and interactions with the sickle hemoglobin gene
    • Steinberg MH, Embury SH. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene. Blood 1986;68:985-990.
    • (1986) Blood , vol.68 , pp. 985-990
    • Steinberg, M.H.1    Embury, S.H.2
  • 6
    • 0028346951 scopus 로고
    • Hb FM-Fort Ripley: Confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing
    • Hain RD, Chitayat D, Cooper R, et al. Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing. Hum Mutat 1994;3:239-242.
    • (1994) Hum Mutat , vol.3 , pp. 239-242
    • Hain, R.D.1    Chitayat, D.2    Cooper, R.3
  • 7
    • 0035543925 scopus 로고    scopus 로고
    • Hb Dartmouth [α66 (E1 5) Leu→Pro (αc2) (CTG→CCG)]: A novel α2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian α-thalassemia-1
    • McBride KL, Snow K, Kubik KS, et al. Hb Dartmouth [α66 (E1 5) Leu→Pro (αc2) (CTG→CCG)]: a novel α2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian α-thalassemia-1. Hemoglobin 2001;25:375-382.
    • (2001) Hemoglobin , vol.25 , pp. 375-382
    • McBride, K.L.1    Snow, K.2    Kubik, K.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.