Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures

X-linked hypophosphatemia (XLH) is a skeletal disease caused by inactivating mutations in the PHEX gene. Mutated or absent PHEX protein/enzyme leads to a decreased serum phosphate level, which cause mineralization defects in the skeleton and teeth (osteomalacia/odontomalacia). It is not yet altogeth...

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Bibliografische gegevens
Gepubliceerd in:J Dent Res
Hoofdauteurs: Coyac, B.R., Hoac, B., Chafey, P., Falgayrac, G., Slimani, L., Rowe, P.S., Penel, G., Linglart, A., McKee, M.D., Chaussain, C., Bardet, C.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: SAGE Publications 2017
Onderwerpen:
Research Reports
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6429567/
https://ncbi.nlm.nih.gov/pubmed/28880715
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034517728497
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