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Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta
Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or qualitatively. The aim of this study was to identify the genetic etiologies of two families presenting with hypomaturation amelogenesis imperfecta. DNA was isolated from periphera...
Tallennettuna:
| Julkaisussa: | Front Physiol |
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| Päätekijät: | , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5397402/ https://ncbi.nlm.nih.gov/pubmed/28473773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2017.00229 |
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