Analysis of CYLD gene variants in 41 patients with multiple familial trichoepithelioma

Documenti analoghi

• Novel variant of the NCSTN gene identified in a woman with hidradenitis suppurativa
  di: Conrad Hempel, et al.
  Pubblicazione: (2025)
• Combination therapy with tofacitinib and minoxidil for Bjornstad syndrome caused by novel BCS1L gene variants
  di: Xiaoxian Li, et al.
  Pubblicazione: (2026)
• Second‐hit somatic variant in a basal cell carcinoma of a basal cell nevus syndrome patient with a germline SUFU variant
  di: Tatsuhiro Noda, et al.
  Pubblicazione: (2025)
• Calcinosis cutis of the lower legs – hyperphosphatemic familial tumoral calcinosis in a patient with GALNT3 mutation
  di: David Ranzinger, et al.
  Pubblicazione: (2025)
• Rare follicular variant of lichen planus pigmentosus and concomitant demodicosis with excellent treatment response
  di: Valentina Faihs, et al.
  Pubblicazione: (2026)