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Disease: Amelogenesis imperfecta pigmented hypomaturation type

  • A novel <em>ODAPH</em> mutation causing amelogenesis imperfecta and its expression in human dental tissues
  • A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues
  • Dental malformations associated with biallelic MMP20 mutations
  • Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant
  • Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation
  • The polarized light microscopy and ultrastructure of Polynesian pigmented tooth enamel
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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