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Volumn 48, Issue 3, 1996, Pages 187-191

Stable inheritance of an HLA-'blank' phenotype associated with a structural mutation in the HLA-A(*)0301 gene

Author keywords

DNA genotyping; HLA A3 HLA A 'blank' non expression; Serology; Transplantation

Indexed keywords

CYSTEINE; DISULFIDE; HLA A ANTIGEN; HLA A3 ANTIGEN; HLA ANTIGEN CLASS 1;

EID: 0029739333     PISSN: 00012815     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0039.1996.tb02627.x     Document Type: Article
Times cited : (37)

References (11)
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  • 2
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    • HLA class I allele (HLA-A2) expression defect associated with a mutation in its enhancer B inverted AT box in two families
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  • 3
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    • HLA-A null allele with a stop codon. HLA-A*0215N, identified in a homozygous state in a healthy adult
    • Ishikawa Y, Tokunaga K, Tanaka H, et al. HLA-A null allele with a stop codon. HLA-A*0215N, identified in a homozygous state in a healthy adult. Immunogenetics 1995: 43: 1-5.
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  • 4
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    • HLA class I variation in Australian Aborigines: Characterisation of allele B*1521
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  • 7
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    • Reptilian class I major histocompatibility complex genes reveal conserved elements in class I structure
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  • 8
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    • Mutation of the α2 domain disulfide bridge of the class I molecule HLA-A*0201. Effect on maturation and peptide presentation
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.