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Mutations in RELT cause autosomal recessive amelogenesis imperfecta
Amelogenesis imperfecta (AI) is a collection of isolated (non‐syndromic) inherited diseases affecting dental enamel formation or a clinical phenotype in syndromic conditions. We characterized three consanguineous AI families with generalized irregular hypoplastic enamel with rapid attrition that per...
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| Publicat a: | Clin Genet |
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| Autors principals: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Blackwell Publishing Ltd
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6392136/ https://ncbi.nlm.nih.gov/pubmed/30506946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.13487 |
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