Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract

مواد مشابهة

• Connexin46 mutations in autosomal dominant congenital cataract.
  بواسطة: Mackay, D, وآخرون
  منشور في: (1999)
• A novel mutation in CRYAB associated with autosomal dominant congenital nuclear cataract in a Chinese family
  بواسطة: Chen, Qiang, وآخرون
  منشور في: (2009)
• A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  بواسطة: Yang, Guoxing, وآخرون
  منشور في: (2011)
• A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family
  بواسطة: Yao, Ke, وآخرون
  منشور في: (2008)
• Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families
  بواسطة: Wang, Zhenyu, وآخرون
  منشور في: (2019)