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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Gaucher, Céline, Boukpessi, Tchilalo, Septier, Dominique, Jehan, Frédéric, Rowe, Peter S., Garabédian, Michèle, Goldberg, Michel, Chaussain-Miller, Catherine
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: S. Karger AG 2008
Pynciau:
Paper
Mynediad Ar-lein: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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