A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family

مواد مشابهة

• Novel mutation of GJA8 in autosomal dominant congenital cataracts
  بواسطة: Ding, Ning, وآخرون
  منشور في: (2020)
• Identification and Functional Analysis of GJA8 Mutation in a Chinese Family with Autosomal Dominant Perinuclear Cataracts
  بواسطة: Su, Dongmei, وآخرون
  منشور في: (2013)
• Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
  بواسطة: Micheal, Shazia, وآخرون
  منشور في: (2018)
• Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract
  بواسطة: Wang, Li, وآخرون
  منشور في: (2011)
• A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
  بواسطة: Zhu, Yanan, وآخرون
  منشور في: (2014)