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Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta
OBJECTIVE: Amelogenesis imperfecta (AI) is a rare hereditary disorder affecting the quality and quantity of the tooth enamel. The purpose of this study was to identify the genetic etiology of hypoplastic AI families based on the candidate gene approach. Materials and methods We recruited three Turki...
Shranjeno v:
| izdano v: | Clin Oral Investig |
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| Main Authors: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2018
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6378126/ https://ncbi.nlm.nih.gov/pubmed/30120606 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00784-018-2577-9 |
| Oznake: |
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