TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies

Eitemau Tebyg

• Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy
  gan: Paliwal, Preeti, et al.
  Cyhoeddwyd: (2010)
• Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort
  gan: Paliwal, Preeti, et al.
  Cyhoeddwyd: (2010)
• Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India
  gan: Gupta, Ranjan, et al.
  Cyhoeddwyd: (2015)
• Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus
  gan: Paliwal, Preeti, et al.
  Cyhoeddwyd: (2011)
• Contact lens rehabilitation following repaired corneal perforations
  gan: Titiyal, Jeewan S, et al.
  Cyhoeddwyd: (2006)