Surprising news: a putative sulfate transporter is defective in Pendred's syndrome

Eur J Endocrinol. 1998 Jun;138(6):623-4. doi: 10.1530/eje.0.1380623.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics*
  • Chromosomes, Human, Pair 7*
  • Cochlea / abnormalities*
  • Genetic Linkage*
  • Goiter / genetics*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Membrane Transport Proteins*
  • Mutation
  • Sulfate Transporters
  • Syndrome
  • Thyroid Gland / physiology

Substances

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