Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications

OBJECTIVE: Hereditary hypophosphatemias (HH) are rare monogenic conditions characterized by decreased renal tubular phosphate reabsorption. The aim of this study was to explore the prevalence, genotypes, phenotypic spectrum, treatment response, and complications of treatment in the Norwegian populat...

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Detalles Bibliográficos
Autores principales: Rafaelsen, Silje, Johansson, Stefan, Ræder, Helge, Bjerknes, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2015
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674593/
https://www.ncbi.nlm.nih.gov/pubmed/26543054
http://dx.doi.org/10.1530/EJE-15-0515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674593/
https://www.ncbi.nlm.nih.gov/pubmed/26543054
http://dx.doi.org/10.1530/EJE-15-0515

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