A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family

Samankaltaisia teoksia

• 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 MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family
  Tekijä: Yu, Yibo, et al.
  Julkaistu: (2014)
• A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  Tekijä: Yang, Guoxing, et al.
  Julkaistu: (2011)
• A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family
  Tekijä: Chen, Qiang, et al.
  Julkaistu: (2009)
• A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families
  Tekijä: Yang, Guoxing, et al.
  Julkaistu: (2011)