Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

Mamm Genome. 1999 May;10(5):520-2. doi: 10.1007/s003359901033.
No abstract available

MeSH terms

  • Animals
  • Blotting, Southern
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 11*
  • Deafness / genetics*
  • Genes, Recessive*
  • Humans
  • Hybrid Cells
  • In Situ Hybridization, Fluorescence
  • Membrane Glycoproteins / genetics*
  • Mice

Substances

  • Membrane Glycoproteins
  • OTOG protein, human
  • Otog protein, mouse