Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract

Những quyển sách tương tự

• Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
  Bằng: Li, Fei-feng, et al.
  Được phát hành: (2008)
• A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract
  Bằng: Yang, Juhua, et al.
  Được phát hành: (2008)
• A Novel CRYBB2 Stopgain Mutation Causing Congenital Autosomal Dominant Cataract in a Chinese Family
  Bằng: Zhou, Yu, et al.
  Được phát hành: (2016)
• A novel truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus
  Bằng: Rao, Yan, et al.
  Được phát hành: (2017)
• A splice site mutation in the PAX6 gene which induces exon skipping causes autosomal dominant inherited aniridia
  Bằng: Weisschuh, Nicole, et al.
  Được phát hành: (2012)