Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome (Q40740453)
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scientific article published on April 2002
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome |
scientific article published on April 2002 |
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Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome (English)
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Anthony P Weetman
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Philip F Watson
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Julie P Taylor
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Russell A Metcalfe
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1 April 2002
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