A mutation in PDS causes non-syndromic recessive deafness

Nat Genet. 1998 Mar;18(3):215-7. doi: 10.1038/ng0398-215.
No abstract available

Publication types

  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Carrier Proteins / genetics
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 7
  • Cochlea / abnormalities
  • Female
  • Genes, Recessive
  • Genetic Linkage
  • Genetic Markers
  • Goiter / genetics*
  • Hearing Loss, Sensorineural / genetics*
  • Homozygote
  • Humans
  • Male
  • Membrane Transport Proteins*
  • Molecular Sequence Data
  • Mutation*
  • Pedigree
  • Sequence Homology, Amino Acid
  • Sulfate Transporters

Substances

  • Carrier Proteins
  • Genetic Markers
  • Membrane Transport Proteins
  • SLC26A4 protein, human
  • Sulfate Transporters