A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

Παρόμοια τεκμήρια

• Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
  ανά: Li, Fei-feng, 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 truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus
  ανά: Rao, Yan, κ.ά.
  Έκδοση: (2017)
• A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q
  ανά: Mackay, Donna S., κ.ά.
  Έκδοση: (2002)
• A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract
  ανά: Yung-Hao Ching, κ.ά.
  Έκδοση: (2019-01-01)