Singleton-Merten Syndrome: a rare autoimmune disorder caused by a specific IFIH1 mutation

Gelijkaardige items

• A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
  door: Rutsch, Frank, et al.
  Gepubliceerd in: (2015)
• MDA5-Associated Neuroinflammation and the Singleton–Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum
  door: Buers, Insa, et al.
  Gepubliceerd in: (2017)
• RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
  door: Lu, Changming, et al.
  Gepubliceerd in: (2017)
• Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi–Goutières and Singleton–Merten syndromes
  door: Bursztejn, A.-C., et al.
  Gepubliceerd in: (2015)
• DDX58 and Classic Singleton-Merten Syndrome
  door: Ferreira, Carlos R., et al.
  Gepubliceerd in: (2018)