Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Ítems similars

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