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Volumn 45, Issue 3, 1999, Pages 426-428

Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; DIAGNOSTIC VALUE; GENE ISOLATION; HEMOCHROMATOSIS; HUMAN; HUMAN CELL; IRON ABSORPTION; IRON METABOLISM; POLYMERASE CHAIN REACTION;

EID: 0032914223     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/45.3.426     Document Type: Article
Times cited : (33)

References (14)
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    • Molecular analysis of HLA-H gene mutations in New Zealand patients with haemochromatosis
    • 5. Burt MJ, Upton JD, Morison IM, Chapman BA, Faed JM, George PM. Molecular analysis of HLA-H gene mutations in New Zealand patients with haemochromatosis. NZ Med J 1997;110:429-32.
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    • A novel MHC class 1-like gene is mutated in patients with hereditary heamochromatosis
    • 8. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, et al. A novel MHC class 1-like gene is mutated in patients with hereditary heamochromatosis. Nat Genet 1996;13:399-408.
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    • Feder, J.N.1    Gnirke, A.2    Thomas, W.3    Tsuchihashi, Z.4    Ruddy, D.A.5    Basava, A.6
  • 9
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    • Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor
    • 9. Lebron JA, Bennett MJ, Vaughn DE, Chirino AJ, Snow PM, Mintier GA, et al. Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor. Cell 1998;93:111-23.
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    • The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.