Adult-onset manifestation of idiopathic T-cell lymphopenia due to a heterozygous RAG1 mutation

Documenti analoghi

• Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis
  di: Walter, Jolan E., et al.
  Pubblicazione: (2014)
• Human RAG mutations: biochemistry and clinical implications
  di: Notarangelo, Luigi D., et al.
  Pubblicazione: (2016)
• RAG1 reversion mosaicism in a patient with Omenn syndrome
  di: Crestani, Elena, et al.
  Pubblicazione: (2014)
• Late Onset Hypomorphic RAG2 Deficiency Presentation with Fatal Vaccine-Strain VZV Infection
  di: Dutmer, Cullen M., et al.
  Pubblicazione: (2015)
• Expanding the spectrum of recombination-activating gene 1 deficiency: A family with early-onset autoimmunity
  di: Henderson, Lauren A., et al.
  Pubblicazione: (2013)