Schnyder Corneal Dystrophy in a Saudi Arabian Family with Heterozygous UBIAD1 Mutation (p.L121F)

Lignende værker

• UBIAD1 Mutation Alters a Mitochondrial Prenyltransferase to Cause Schnyder Corneal Dystrophy
  af: Nickerson, Michael L., et al.
  Udgivet: (2010)
• A mutation in the UBIAD1 gene in a Han Chinese family with Schnyder corneal dystrophy
  af: Du, Chunyu, et al.
  Udgivet: (2011)
• Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy
  af: Lin, Benjamin R., et al.
  Udgivet: (2016)
• Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene
  af: Evans, Cerys J., et al.
  Udgivet: (2018)
• Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy
  af: Orr, Andrew, et al.
  Udgivet: (2007)