In utero and early postnatal presentation of autoimmune lymphoproliferative syndrome in a family with a novel FAS mutation

פריטים דומים

• FAS Haploinsufficiency Is a Common Disease Mechanism in the Human Autoimmune Lymphoproliferative Syndrome
  מאת: Kuehn, Hye Sun, et al.
  יצא לאור: (2011)
• Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome
  מאת: Dowdell, Kennichi C., et al.
  יצא לאור: (2010)
• Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome
  מאת: Caminha, Iusta, et al.
  יצא לאור: (2010)
• Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations
  מאת: Price, Susan, et al.
  יצא לאור: (2014)
• Bone marrow findings in autoimmune lymphoproliferative syndrome with germline FAS mutation
  מאת: Xie, Yi, et al.
  יצא לאור: (2017)