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Identification of the C-terminal region in Amelogenesis Imperfecta causative protein WDR72 required for Golgi localization
Amelogenesis Imperfecta (AI) represents a group of hereditary conditions that manifest tooth enamel defects. Several causative mutations in the WDR72 gene have been identified and patients with WDR72 mutations have brown (or orange-brown) discolored enamel, rough enamel surface, early loss of enamel...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930991/ https://www.ncbi.nlm.nih.gov/pubmed/35301423 http://dx.doi.org/10.1038/s41598-022-08719-7 |