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Unusual T cell clones in a patient with Nijmegen breakage syndrome.

The rare autosomal recessive Nijmegen breakage syndrome is characterised by severe immunodeficiency, microcephaly associated with mental retardation, and typical chromosomal rearrangements in peripheral T lymphocytes. This syndrome, though similar to ataxia telangiectasia, does not exhibit the neuro...

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Main Authors: Stoppa-Lyonnet, D, Girault, D, LeDeist, F, Aurias, A
格式: Artigo
語言:Inglês
出版: 1992
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015857/
https://ncbi.nlm.nih.gov/pubmed/1613764
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