Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification

Dentinogenesis imperfecta is an autosomal dominant disease characterized by severe hypomineralization of dentin and altered dentin structure. Dentin extra cellular matrix is composed of 90% of collagen type I and 10% of non-collagenous proteins among which dentin sialoprotein (DSP), dentin glycoprot...

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Bibliographic Details
Published in:Eur J Hum Genet
Main Authors: de La Dure-Molla, Muriel, Philippe Fournier, Benjamin, Berdal, Ariane
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 2015
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Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4666581/
https://ncbi.nlm.nih.gov/pubmed/25118030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.159
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