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Familial hypocalciuric hypercalcemia caused by homozygous CaSR gene mutation: A case report of a family

INTRODUCTION: Familial hypocalciuric hypercalcemia (FHH) is a group of autosomal dominant genetic diseases with persistent hypercalcemia and hypocalciuria. The calcium-sensitive receptor (CaSR) plays an important role in calcium and phosphorus metabolism. PATIENT CONCERNS: A 32-year-old man who had...

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Detalles Bibliográficos
Autores principales:	Wang, Feifei, Hu, Jia, Mei, Chao, Lin, Xia, Zhang, Ling
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2020
Materias:	4300
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458196/ https://www.ncbi.nlm.nih.gov/pubmed/32871939 http://dx.doi.org/10.1097/MD.0000000000021940

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