Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts

Ítems similars

• A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families
  per: Yang, Guoxing, et al.
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• A mutated CRYGD associated with congenital coralliform cataracts in two Chinese pedigrees
  per: Cai, Su-Ping, et al.
  Publicat: (2021)
• Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts
  per: Nandrot, E, et al.
  Publicat: (2003)
• Mutation analysis of CRYAA, CRYGC, and CRYGD associated with autosomal dominant congenital cataract in Brazilian families
  per: Santana, Alessandro, et al.
  Publicat: (2009)
• A novel human CRYGD mutation in a juvenile autosomal dominant cataract
  per: Roshan, Mascarenhas, et al.
  Publicat: (2010)