Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

類似資料

• Identification of three ADA2 deficiency families with novel CECR1 mutations
  著者:: Sarrabay, G, 等
  出版事項: (2015)
• Impaired interferon signature in severe COVID-19
  著者:: Gruber, Conor
  出版事項: (2020)
• Transcriptome Analysis of the Interferon-Signature Defining the Autoimmune Process of Sjögren’s Syndrome
  著者:: Peck, A. B., 等
  出版事項: (2012)
• Mutations in CECR1 associated with a neutrophil signature in peripheral blood
  著者:: Belot, Alexandre, 等
  出版事項: (2014)
• OR13-001 Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes
  著者:: Zhou, Q, 等
  出版事項: (2013)