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Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta
OBJECTIVE: Hereditary defects in tooth enamel formation, amelogenesis imperfecta (AI), can be non-syndromic or syndromic phenotype. Integrins are signaling proteins that mediate cell–cell and cell–extracellular matrix communication, and their involvement in tooth development is well known. The purpo...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Oral Dis |
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| Κύριοι συγγραφείς: | , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Blackwell Publishing Ltd
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4440386/ https://ncbi.nlm.nih.gov/pubmed/25431241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/odi.12303 |
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