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A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome

2013-01-01

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Literature Corpus work
92c0b4bf-3f33-5a38-94ea-1de596c7ce6a
DOI
10.1186/1687-9856-2013-s1-p170
PMCID
PMC3850142
Open publication

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A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndromeDOI 10.1186/1687-9856-2013-s1-p170
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