Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus

Hum Genet. 2007 Nov;122(3-4):414.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Codon / genetics
  • Cytoskeletal Proteins / genetics*
  • Humans
  • Membrane Proteins / genetics*
  • Mutation, Missense
  • Nystagmus, Congenital / genetics*

Substances

  • Codon
  • Cytoskeletal Proteins
  • FRMD7 protein, human
  • Membrane Proteins