Original languageEnglish
Pages (from-to)101-107
Number of pages7
JournalOphthalmic Genetics
Volume38
Issue number2
DOIs
Publication statusPublished - 2017

Keywords

  • 6p25 deletion
  • Axenfeld-Rieger syndrome
  • neurocristopathy
  • AXENFELD-RIEGER-SYNDROME
  • SUBTELOMERE DELETION
  • FOXC1
  • PHENOTYPE
  • GLAUCOMA
  • SPECTRUM
  • MUTATIONS
  • PITX2
  • FOXF2
  • GENE

Cite this