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Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

Autoimmune lymphoproliferative syndrome (ALPS) is characterized by childhood onset of lymphadenopathy, hepatosplenomegaly, autoimmune cytopenias, elevated numbers of double-negative T (DNT) cells, and increased risk of lymphoma. Most cases of ALPS are associated with germline mutations of the FAS ge...

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Detalhes bibliográficos
Main Authors: Dowdell, Kennichi C., Niemela, Julie E., Price, Susan, Davis, Joie, Hornung, Ronald L., Oliveira, João Bosco, Puck, Jennifer M., Jaffe, Elaine S., Pittaluga, Stefania, Cohen, Jeffrey I., Fleisher, Thomas A., Rao, V. Koneti
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2892951/
https://ncbi.nlm.nih.gov/pubmed/20360470
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2010-01-263145
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