Severe combined immunodeficiency caused by deficiency in either the δ or the ε subunit of CD3

We investigated the molecular mechanism underlying a severe combined immunodeficiency characterized by the selective and complete absence of T cells. The condition was found in 5 patients and 2 fetuses from 3 consanguineous families. Linkage analysis performed on the 3 families revealed that the pat...

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Detalhes bibliográficos
Main Authors: Basile, Geneviève de Saint, Geissmann, Frédéric, Flori, Elisabeth, Uring-Lambert, Béatrice, Soudais, Claire, Cavazzana-Calvo, Marina, Durandy, Anne, Jabado, Nada, Fischer, Alain, Deist, Françoise Le
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2004
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC525745/
https://ncbi.nlm.nih.gov/pubmed/15546002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200422588
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