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A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
“Amelogenesis imperfecta” (AI) describes a group of genetic conditions that result in defects in tooth enamel formation. Mutations in many genes are known to cause AI, including the gene encoding the serine protease, kallikrein related peptidase 4 (KLK4), expressed during the maturation stage of ame...
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| Τόπος έκδοσης: | Front Physiol |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5447068/ https://ncbi.nlm.nih.gov/pubmed/28611678 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2017.00333 |
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