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A hereditary immunodeficiency characterized by CD8+ T lymphocyte deficiency and impaired lymphocyte activation.

An unusual form of severe combined immunodeficiency in children from two different families was associated with absence of CD8+ T lymphocytes and normal numbers of CD4+ T lymphocytes that did not respond to stimulation by non-specific mitogens, specific antibodies against T cell receptor or specific...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Monafo, W J, Polmar, S H, Neudorf, S, Mather, A, Filipovich, A H
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1992
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1554576/
https://ncbi.nlm.nih.gov/pubmed/1333922
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