Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Eitemau Tebyg

• MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
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  Cyhoeddwyd: (2005)
• Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
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  Cyhoeddwyd: (2009)
• Mutations in RELT cause autosomal recessive amelogenesis imperfecta
  gan: Kim, Jung‐Wook, et al.
  Cyhoeddwyd: (2018)
• Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
  gan: Hart, T, et al.
  Cyhoeddwyd: (2003)
• An autosomal recessive cone–rod dystrophy associated with amelogenesis imperfecta
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  Cyhoeddwyd: (2004)