(Q40740453)
Statements
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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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87
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4
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1778-1784
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Identifiers
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