A novel missense pathogenic variant in the CYLD gene in a Chinese family with multiple familial trichoepithelioma

Ähnliche Einträge

• A novel splicing CYLD variant associated with trichoepithelioma papulosum multiplex demonstrating intrafamilial severity variability
  von: Ryo Fukaura, et al.
  Veröffentlicht: (2024)
• Analysis of CYLD gene variants in 41 patients with multiple familial trichoepithelioma
  von: Mengxing Cui, et al.
  Veröffentlicht: (2026)
• CYLD novel splicing mutation in a patient with CYLD cutaneous syndrome with basal cell carcinomas
  von: Jiro Nishio, et al.
  Veröffentlicht: (2024)
• Two novel mutations in LSS gene associated with hypotrichosis simplex in a Chinese family
  von: Linfang Yang, et al.
  Veröffentlicht: (2024)
• Variations in RASA1 and EPHB4 in Chinese patients with capillary malformation‐arteriovenous malformation
  von: Qin Zeng, et al.
  Veröffentlicht: (2024)