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A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
Wong, SMY, But, WM, Chan, Angel, Chan, WVolume:
2013
Language:
english
Journal:
International Journal of Pediatric Endocrinology
DOI:
10.1186/1687-9856-2013-S1-P170
Date:
October, 2013
File:
PDF, 333 KB
english, 2013