A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree

समान संसाधन

• A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea
  द्वारा: Zhang, Lu, और अन्य
  प्रकाशित: (2009)
• A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family
  द्वारा: Yao, Ke, और अन्य
  प्रकाशित: (2008)
• A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese family
  द्वारा: Yang, Zhenfei, और अन्य
  प्रकाशित: (2012)
• A G→T splice site mutation of CRYBA1/A3 associated with autosomal dominant suture cataracts in a Chinese family
  द्वारा: Yang, Zhenfei, और अन्य
  प्रकाशित: (2011)
• A novel mutation in CRYAA is associated with autosomal dominant suture cataracts in a Chinese family
  द्वारा: Su, Dongmei, और अन्य
  प्रकाशित: (2012)