PHENOTYPIC DIFFERENCES BETWEEN MICE DEFICIENT IN XIAP AND SAP, TWO FACTORS TARGETED IN X-LINKED LYMPHOPROLIFERATIVE SYNDROME (XLP)

Mutations in the X-linked inhibitor of apoptosis (XIAP) have recently been identified in patients with the rare genetic disease, X-linked lymphoproliferative syndrome (XLP), which was previously thought to be solely attributable to mutations in a distinct gene, SAP. To further understand the roles o...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Rumble, Julie M., Oetjen, Karolyn A., Stein, Paul L., Schwartzberg, Pamela L., Moore, Bethany B., Duckett, Colin S.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2009
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2744477/
https://ncbi.nlm.nih.gov/pubmed/19595300
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cellimm.2009.05.017
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