Novel mutations in CRYGD are associated with congenital cataracts in Chinese families

類似資料

• A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families
  著者:: Yang, Guoxing, 等
  出版事項: (2011)
• A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  著者:: Yang, Guoxing, 等
  出版事項: (2011)
• A recurrent mutation in CRYBA1 is associated with an autosomal dominant congenital nuclear cataract disease in a Chinese family
  著者:: Yang, Guoxing, 等
  出版事項: (2011)
• A mutated CRYGD associated with congenital coralliform cataracts in two Chinese pedigrees
  著者:: Cai, Su-Ping, 等
  出版事項: (2021)
• A Novel Insertion Variant of CRYGD Is Associated with Congenital Nuclear Cataract in a Chinese Family
  著者:: Zhuang, Xiaotong, 等
  出版事項: (2015)