A novel truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus

Παρόμοια τεκμήρια

• A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract
  ανά: Yang, Juhua, κ.ά.
  Έκδοση: (2008)
• Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract
  ανά: Weisschuh, Nicole, κ.ά.
  Έκδοση: (2012)
• A Novel CRYBB2 Stopgain Mutation Causing Congenital Autosomal Dominant Cataract in a Chinese Family
  ανά: Zhou, Yu, κ.ά.
  Έκδοση: (2016)
• A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract
  ανά: Yung-Hao Ching, κ.ά.
  Έκδοση: (2019-01-01)
• Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
  ανά: Li, Fei-feng, κ.ά.
  Έκδοση: (2008)