MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Ítems similars

• Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
  per: Hart, P, et al.
  Publicat: (2004)
• MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta
  per: Ozdemir, D., et al.
  Publicat: (2005)
• Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta
  per: Kim, Youn Jung, et al.
  Publicat: (2017)
• Mutations in RELT cause autosomal recessive amelogenesis imperfecta
  per: Kim, Jung‐Wook, et al.
  Publicat: (2018)
• Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
  per: El-Sayed, Walid, et al.
  Publicat: (2009)