Mutations in the pendred syndrome (PDS/SLC26A) gene: An increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia

Peter Kopp*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

22 Scopus citations
Original languageEnglish (US)
Pages (from-to)67-69
Number of pages3
JournalJournal of clinical endocrinology and metabolism
Volume99
Issue number1
DOIs
StatePublished - Jan 2014

ASJC Scopus subject areas

  • Biochemistry, medical
  • Endocrinology
  • Biochemistry
  • Clinical Biochemistry
  • Endocrinology, Diabetes and Metabolism

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