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Volumn 27, Issue 5, 1997, Pages 773-779

Predominance of the HLA-H Cys282Tyr mutation in austrian patients with genetic haemochromatosis

Author keywords

Genetic haemochromatosis; HLA H; Mutation; Polymorphism

Indexed keywords

ADULT; AGAR GEL ELECTROPHORESIS; ARTICLE; AUSTRIA; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HEMOCHROMATOSIS; HLA SYSTEM; HUMAN; HUMAN CELL; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TELOMERE; TISSUE INJURY;

EID: 18144444007     PISSN: 01688278     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-8278(97)80312-1     Document Type: Article
Times cited : (86)

References (17)
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    • Haplotype analysis in Australian hemochromatosis patients - Evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.