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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author Wong, SMY
But, WM
Chan, Angel
Chan, W
author_facet Wong, SMY
But, WM
Chan, Angel
Chan, W
author_sort Wong, SMY
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spelling pubmed-38501422013-12-17 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, W Int J Pediatr Endocrinol Poster Presentation BioMed Central 2013 2013-10-03 /pmc/articles/PMC3850142/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P170 Text en Copyright © 2013 Wong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Presentation
Wong, SMY
But, WM
Chan, Angel
Chan, W
A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title_full A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title_fullStr A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title_full_unstemmed A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title_short A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
title_sort rare cause of primary hypoparathyroidism due to a novel mutation in the gata3 gene – the barakat syndrome
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850142/
http://dx.doi.org/10.1186/1687-9856-2013-S1-P170
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