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

समान संसाधन

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