A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia

The syndrome of hereditary 1,25-dihydroxyvitamin D–resistant rickets (HVDRR) is a genetic disease of altered mineral homeostasis due to mutations in the vitamin D receptor (VDR) gene. It is frequently, but not always, accompanied by the presence of alopecia. Mouse models that recapitulate this syndr...

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Detalhes bibliográficos
Main Authors: Lee, Seong Min, Goellner, Joseph J., O'Brien, Charles A., Pike, J. Wesley
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2014
Assuntos:
Calcium-Regulating Hormones
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4197979/
https://ncbi.nlm.nih.gov/pubmed/25147982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/en.2014-1417
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