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A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene

We experienced a case of familial hypoparathyroidism with an autosomal dominant pattern of transmission and performed molecular analysis of the calcium-sensing receptor (CASR) gene. The patient was a female neonate, born by cesarean section at term because of breech presentation. Her mother had been...

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Detalles Bibliográficos
Autores principales:	Miyata, Ichiro, Yoshikawa, Hideki, Kurokawa, Naokiyo, Kanno, Kei-ichi, Hayashi, Yoshihiro, Eto, Yoshikatsu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Japanese Society for Pediatric Endocrinology 2008
Materias:	Original
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004876/ https://www.ncbi.nlm.nih.gov/pubmed/24790357 http://dx.doi.org/10.1297/cpe.17.17

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