Autosomal dominant amelogenesis imperfecta associated with ENAM frameshift mutation p.Asn36Ilefs56

Antzeko izenburuak

• Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
  nork: Hart, T, et al.
  Argitaratua: (2003)
• FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta
  nork: Wang, S.K., et al.
  Argitaratua: (2020)
• Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta
  nork: Sandra Gutiérrez, et al.
  Argitaratua: (2012-01-01)
• Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta
  nork: Gutiérrez, Sandra, et al.
  Argitaratua: (2012)
• Translational Attenuation by an Intron Retention in the 5′ UTR of ENAM Causes Amelogenesis Imperfecta
  nork: Kim, Youn Jung, et al.
  Argitaratua: (2021)