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Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
Pachyonychia congenita (PC) is a cutaneous disorder primarily characterized by nail dystrophy and painful palmoplantar keratoderma. PC is caused by mutations in KRT6A, KRT6B, KRT6C, KRT16, and KRT17, a set of keratin genes expressed in the nail bed, palmoplantar epidermis, oral mucosal epithelium, h...
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| Publicado en: | PLoS Genet |
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| Autores principales: | , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Public Library of Science
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5794186/ https://ncbi.nlm.nih.gov/pubmed/29357356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007168 |
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