MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Παρόμοια τεκμήρια

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