Homozygous mutation (L527R) of TGFBI in an individual with lattice corneal dystrophy

समान संसाधन

• Double mutation (R124H, N544S) of TGFBI in two sisters with combined expression of Avellino and lattice corneal dystrophies
  द्वारा: Yamada, Naoyuki, और अन्य
  प्रकाशित: (2009)
• A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the TGFBI Gene
  द्वारा: Kim, Jinsun, और अन्य
  प्रकाशित: (2014)
• Unique TGFBI Protein in Lattice Corneal Dystrophy
  द्वारा: Han, Yu-Ping, और अन्य
  प्रकाशित: (2011)
• Granular and Lattice Deposits in Corneal Dystrophy Caused by R124C Mutation of TGFBI
  द्वारा: Patel, D.A., और अन्य
  प्रकाशित: (2010)
• Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene
  द्वारा: Afshari, Natalie A., और अन्य
  प्रकाशित: (2008)