Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families

Clin Genet. 2007 Sep;72(3):261-3. doi: 10.1111/j.1399-0004.2007.00852.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Female
  • Frameshift Mutation
  • Genes, Recessive
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Iran
  • Male
  • Mutation, Missense
  • Nerve Tissue Proteins / genetics*
  • Pedigree

Substances

  • Nerve Tissue Proteins
  • PJVK protein, human