Dentin Noncollagenous Matrix Proteins in Familial Hypophosphatemic Rickets

Familial hypophosphatemic rickets is transmitted in most cases as an X-linked dominant trait and results from the mutation of the PHEX gene predominantly expressed in osteoblast and odontoblast. Patients with rickets have been reported to display important dentin defects. Our purpose was to explore...

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Auteurs principaux: Gaucher, Céline, Boukpessi, Tchilalo, Septier, Dominique, Jehan, Frédéric, Rowe, Peter S., Garabédian, Michèle, Goldberg, Michel, Chaussain-Miller, Catherine
Format: Artigo
Langue:Inglês
Publié: S. Karger AG 2008
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Paper
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3352030/
https://ncbi.nlm.nih.gov/pubmed/18701809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000151382
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