Novel mutation of GJA8 in autosomal dominant congenital cataracts

Samankaltaisia teoksia

• Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
  Tekijä: Micheal, Shazia, et al.
  Julkaistu: (2018)
• A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
  Tekijä: Willoughby, C, et al.
  Julkaistu: (2003)
• A novel GJA3 mutation causing autosomal dominant congenital perinuclear cataracts
  Tekijä: Yanan Zhu, et al.
  Julkaistu: (2025-04-01)
• A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
  Tekijä: Zhu, Yanan, et al.
  Julkaistu: (2014)
• Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract.
  Tekijä: Yanan Zhu, et al.
  Julkaistu: (2015-01-01)