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

Ítems similars

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