Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization

CONTEXT: Type VIII osteogenesis imperfecta (OI; OMIM 601915) is a recessive form of lethal or severe OI caused by null mutations in P3H1, which encodes prolyl 3-hydroxylase 1. OBJECTIVES: Clinical and bone material description of non-lethal type VIII OI. DESIGN: Natural history study of type VIII OI...

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Foilsithe in:J Clin Endocrinol Metab
Main Authors: Fratzl-Zelman, Nadja, Barnes, Aileen M., Weis, MaryAnn, Carter, Erin, Hefferan, Theresa E., Perino, Giorgio, Chang, Weizhong, Smith, Peter A., Roschger, Paul, Klaushofer, Klaus, Glorieux, Francis H., Eyre, David R., Raggio, Cathleen, Rauch, Frank, Marini, Joan C.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Endocrine Society 2016
Ábhair:
Original Articles
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5010570/
https://ncbi.nlm.nih.gov/pubmed/27383115
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2016-1334
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