Congenital hypothyroidism as the initial presentation of pendred syndrome associated with mutated IVS7-2A>G in SLC26A4 gene in a Taiwanese neonate

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)94-95
Number of pages2
JournalPediatrics and Neonatology
Issue number1
Publication statusPublished - 2023 Jan

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health

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