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

Ítems similars

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