Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus

Ophthalmic Genet. 2009 Dec;30(4):206-7. doi: 10.3109/13816810903183613.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant
  • Kinesins / genetics*
  • Male
  • Mutation*
  • Open Reading Frames
  • Polymerase Chain Reaction
  • Strabismus / congenital
  • Strabismus / genetics*

Substances

  • Homeodomain Proteins
  • KIF21A protein, human
  • PHOX2A protein, human
  • Kinesins