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Routine HLA‐B genotyping with PCR‐sequence‐specific oligonucleotides (PCR‐SSO) detects eight new alleles: B*0807, B*0809, B*1551, B*3529, B*3532, B*4025, B*5304 and B*5508
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2000
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HlaHistocompatibilityGeneticsImmunodeficienciesImmunologyHla ImmunogeneticsPathologyImmunodominanceHuman PolymorphismMolecular GeneticsGenomicsPeptide BindingImmunotherapyNew AllelesImmune-related Gene PolymorphismNew PolymorphismsImmunogeneticsMolecular DiagnosticsCell TransplantationTransplantationAutoimmune DiseaseHuman Leukocyte AntigenAutoimmunityGenetic VariationAllelic VariantMolecular Diagnostic TechniquesRoutine Hla‐bPcr‐sequence‐specific OligonucleotidesHla TypingMedicine
This paper describes eight new alleles (B*0807, B*0809, B*1551, B*3529, B*3532, B*4025, B*5304 and B*5508) that have been found by routine HLA-B genotyping with sequence-specific oligonucleotides (SSOs). All of the new alleles have variations which cause changes in residues that occur within antigen binding pockets and T-cell recognition sites of the antigen. The new polymorphisms within these new alleles may affect the nature and specificity of peptide binding and cause differential T-cell activation, which may have an affect in transplantation.
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