Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)

Podobne zapisy

• Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing
  od: Engelhardt, Karin R., i wsp.
  Wydane: (2016)
• Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
  od: Acres, Meghan J., i wsp.
  Wydane: (2019)
• Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation
  od: Mulhern, Ciara M., i wsp.
  Wydane: (2019)
• African-Derived Genetic Polymorphisms in TNFAIP3 Mediate Risk for Autoimmunity
  od: Lodolce, James P., i wsp.
  Wydane: (2010)
• Sequencing of TNFAIP3 and Association of Variants with Multiple Autoimmune Diseases
  od: Musone, Stacy L, i wsp.
  Wydane: (2011)