Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome

Similar Items

• A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
  od: Wu, Xing, i dr.
  Izdano: (2019)
• Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
  od: Tümer, Zeynep, i dr.
  Izdano: (2009)
• A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
  od: Micheal, Shazia, i dr.
  Izdano: (2016)
• The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning
  od: Chrystal, Paul W., i dr.
  Izdano: (2021)
• Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome
  od: Valeria Lo Faro, i dr.
  Izdano: (2020-07-01)