A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome

Lignende værker

• Identification and functional study of a novel FOXC1 missense mutation in a Chinese family with Axenfeld–Rieger syndrome
  af: Xue Gong, et al.
  Udgivet: (2025-06-01)
• A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome
  af: Li, Dandan, et al.
  Udgivet: (2008)
• Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
  af: Tümer, Zeynep, et al.
  Udgivet: (2009)
• Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome
  af: Fuse, Nobuo, et al.
  Udgivet: (2007)
• A Chinese family with Axenfeld-Rieger syndrome: report of the clinical and genetic findings
  af: Sun, Da-Peng, et al.
  Udgivet: (2017)