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