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Volumn 45, Issue 11, 1999, Pages 2025-2026

Denaturing gradient gel electrophoresis analysis of the hemochromatosis (HFE) gene: Impact of HFE gene mutations on the manifestation of porphyria cutanea tarda

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL FEATURE; DENATURING GRADIENT GEL ELECTROPHORESIS; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HEMOCHROMATOSIS; HUMAN; MAJOR CLINICAL STUDY; PORPHYRIA CUTANEA TARDA; SEQUENCE ANALYSIS;

EID: 0032733817     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/45.11.2025     Document Type: Article
Times cited : (15)

References (12)
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  • 5
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    • The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients
    • 5. Stuart KA, Busfield F, Jazwinska EC, Gibson P, Butterworth LA, Cooksley WG, et al. The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients. J Hepatol 1998;28:404-9.
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  • 6
    • 0031982781 scopus 로고    scopus 로고
    • High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda
    • 6. Sampietro M, Piperno A, Lupica L, Arosio C, Vergani A, Corbetta N, et al. High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda [see comments]. Hepatology 1998;27:181-4.
    • (1998) Hepatology , vol.27 , pp. 181-184
    • Sampietro, M.1    Piperno, A.2    Lupica, L.3    Arosio, C.4    Vergani, A.5    Corbetta, N.6
  • 7
    • 0032464908 scopus 로고    scopus 로고
    • Are His63Asp or Cys282Tyr HFE mutations associated with porphyria cutanea tarda? Data of patients from central and southern Italy
    • 7. D'Amato M, Macri A, Griso D, Biolcati G, Ameglio F. Are His63Asp or Cys282Tyr HFE mutations associated with porphyria cutanea tarda? Data of patients from central and southern Italy [Letter]. J Investig Dermatol 1998;111:1241-2.
    • (1998) J Investig Dermatol , vol.111 , pp. 1241-1242
    • D'Amato, M.1    Macri, A.2    Griso, D.3    Biolcati, G.4    Ameglio, F.5
  • 8
    • 0032231331 scopus 로고    scopus 로고
    • Familial porphyria cutanea tarda: Characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis alleles
    • 8. Mendez M, Sorkin L, Rossetti MV, Astrin KH, del C Batlle AM, Parera VE, et al. Familial porphyria cutanea tarda: characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis alleles. Am J Hum Genet 1998;63:1363-75.
    • (1998) Am J Hum Genet , vol.63 , pp. 1363-1375
    • Mendez, M.1    Sorkin, L.2    Rossetti, M.V.3    Astrin, K.H.4    Del C Batlle, A.M.5    Parera, V.E.6
  • 10
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    • HFE mutations analysis in 711 hemochromatosis probands: Evidence for S65C implication in mild form of hemochromatosis
    • 10. Mura C, Raguenes O, Ferec C. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis. Blood 1999;93:2502-5.
    • (1999) Blood , vol.93 , pp. 2502-2505
    • Mura, C.1    Raguenes, O.2    Ferec, C.3
  • 11
    • 0031715898 scopus 로고    scopus 로고
    • Determination of gene frequencies for two common haemochromatosis mutations in the Danish population by a novel polymerase chain reaction with sequence-specific primers
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  • 12
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    • (1997) Hum Mutat , vol.9 , pp. 122-130
    • Nissen, H.1    Petersen, N.E.2    Mustajoki, S.3    Hansen, T.S.4    Mustajoki, P.5    Kauppinen, R.6    Hørder, M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.