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

Samankaltaisia teoksia

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