Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma

Lignende værker

• Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.
  af: Bejjani, B A, et al.
  Udgivet: (1998)
• Axenfeld-Rieger Syndrome Associated with Congenital Glaucoma and Cytochrome P4501B1 Gene Mutations
  af: Tanwar, Mukesh, et al.
  Udgivet: (2010)
• Herbicide-resistant tobacco plants expressing the fused enzyme between rat cytochrome P4501A1 (CYP1A1) and yeast NADPH-cytochrome P450 oxidoreductase.
  af: Shiota, N, et al.
  Udgivet: (1994)
• Regulation of Human Cytochrome P4501A1 (hCYP1A1): A Plausible Target for Chemoprevention?
  af: Santes-Palacios, Rebeca, et al.
  Udgivet: (2016)
• Primary Congenital Glaucoma and the Involvement of CYP1B1
  af: Kaur, Kiranpreet, et al.
  Udgivet: (2011)