Studies on Axenfeld–Rieger syndrome patients and mice reveal Foxc1's role in corneal neovascularization

Ítems similars

• Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
  per: Tümer, Zeynep, et al.
  Publicat: (2009)
• Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome
  per: Fuse, Nobuo, et al.
  Publicat: (2007)
• The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning
  per: Chrystal, Paul W., et al.
  Publicat: (2021)
• A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
  per: Wu, Xing, et al.
  Publicat: (2019)
• The Axenfeld syndrome and the Rieger syndrome.
  per: Fitch, N, et al.
  Publicat: (1978)