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

✍ Scribed by Wong, SMY; But, WM; Chan, Angel; Chan, W

Book ID: 121617324
Publisher: BioMed Central
Year: 2013
Tongue: English
Weight: 333 KB
Volume: 2013
Category: Article
ISSN: 1687-9848
DOI: 10.1186/1687-9856-2013-S1-P170

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