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

Detalles Bibliográficos
Autores principales:	Wong, SMY, But, WM, Chan, Angel, Chan, W
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850142/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P170

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