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

Peter Kopp

doi:10.1210/jc.2013-4319

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

Medicine, Endocrinology Division

Research output: Contribution to journal › Review article › peer-review

18 Scopus citations

Original language	English (US)
Pages (from-to)	67-69
Number of pages	3
Journal	Journal of Clinical Endocrinology and Metabolism
Volume	99
Issue number	1
DOIs	https://doi.org/10.1210/jc.2013-4319
State	Published - Jan 2014

ASJC Scopus subject areas

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1210/jc.2013-4319

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

ASJC Scopus subject areas

UN SDGs

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