Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia

J Clin Endocrinol Metab. 2014 Jan;99(1):67-9. doi: 10.1210/jc.2013-4319.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Congenital Hypothyroidism / genetics*
  • Female
  • Humans
  • Male
  • Membrane Transport Proteins / genetics*
  • Sulfate Transporters
  • Thyroid Dysgenesis / genetics*

Substances

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