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Identification and physical mapping of a polymorphic human T cell receptor V beta gene with a frequent null allele

Germline variation in genes that encode the human T cell receptors (TCRs) may have an important influence in shaping the immune T cell repertoire. In this report we describe a frequent null allele of the human V beta 18 gene, resulting from a nucleotide substitution that creates a stop codon (CGA<...

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Formato: Artigo
Lenguaje:Inglês
Publicado: The Rockefeller University Press 1993
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2190858/
https://ncbi.nlm.nih.gov/pubmed/7678110
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