A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families

Παρόμοια τεκμήρια

• Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts
  ανά: Li, Feifeng, κ.ά.
  Έκδοση: (2008)
• A mutated CRYGD associated with congenital coralliform cataracts in two Chinese pedigrees
  ανά: Cai, Su-Ping, κ.ά.
  Έκδοση: (2021)
• Novel mutations in CRYGD are associated with congenital cataracts in Chinese families
  ανά: Yang, Guoxing, κ.ά.
  Έκδοση: (2016)
• A recurrent mutation in CRYBA1 is associated with an autosomal dominant congenital nuclear cataract disease in a Chinese family
  ανά: Yang, Guoxing, κ.ά.
  Έκδοση: (2011)
• A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  ανά: Yang, Guoxing, κ.ά.
  Έκδοση: (2011)