Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia

Familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant disorder, associated with inactivating mutations of the calcium-sensing receptor (CaSR). To evaluate the functional significance of a CaSR mutation, identified in a young infant who presented with hypercalcemia and hypocalciuria. Th...

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Detalles Bibliográficos
Autores principales: Papadopoulou, Anna, Gole, Evangelia, Melachroinou, Katerina, Meristoudis, Christos, Siahanidou, Tania, Papadimitriou, Anastasios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096500/
https://www.ncbi.nlm.nih.gov/pubmed/27087013
http://dx.doi.org/10.4274/jcrpe.2800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096500/
https://www.ncbi.nlm.nih.gov/pubmed/27087013
http://dx.doi.org/10.4274/jcrpe.2800

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