Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort

Eitemau Tebyg

• TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies
  gan: Paliwal, Preeti, et al.
  Cyhoeddwyd: (2010)
• Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy
  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)
• Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
  gan: Kumawat, Babu Lal, et al.
  Cyhoeddwyd: (2016)
• Need for optical and low vision services for children in schools for the blind in North India
  gan: Pal Nikhil, et al.
  Cyhoeddwyd: (2006-01-01)