Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract

Những quyển sách tương tự

• Novel mutation of GJA8 in autosomal dominant congenital cataracts
  Bằng: Ding, Ning, et al.
  Được phát hành: (2020)
• Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
  Bằng: Micheal, Shazia, et al.
  Được phát hành: (2018)
• A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
  Bằng: Willoughby, C, et al.
  Được phát hành: (2003)
• Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
  Bằng: Li Wang, et al.
  Được phát hành: (2016-01-01)
• Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
  Bằng: Wang, Li, et al.
  Được phát hành: (2016)