A missense mutation in CRYBA4 associated with congenital cataract and microcornea

Benzer Materyaller

• A novel mutation in GJA8 causing congenital cataract–microcornea syndrome in a Chinese pedigree
  Yazar:: Hu, Shanshan, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)
  Yazar:: Zhou, Zhou, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree
  Yazar:: Ding, Xuchen, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)
• A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract
  Yazar:: Ding, Xuchen, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Mutational screening of six genes in Chinese patients with congenital cataract and microcornea
  Yazar:: Sun, Wenmin, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)