A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

Παρόμοια τεκμήρια

• Novel mutation of GJA8 in autosomal dominant congenital cataracts
  ανά: Ding, Ning, κ.ά.
  Έκδοση: (2020)
• Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
  ανά: Micheal, Shazia, κ.ά.
  Έκδοση: (2018)
• Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
  ανά: Li Wang, κ.ά.
  Έκδοση: (2016-01-01)
• Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract
  ανά: Wang, Li, κ.ά.
  Έκδοση: (2011)
• A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
  ανά: Zhu, Yanan, κ.ά.
  Έκδοση: (2014)