SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy

Eitemau Tebyg

• Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome
  gan: Siddiqui, Salina, et al.
  Cyhoeddwyd: (2013)
• Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
  gan: Kumawat, Babu Lal, et al.
  Cyhoeddwyd: (2016)
• Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature
  gan: Kodaganur, Srinivas Gopinath, et al.
  Cyhoeddwyd: (2013)
• Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11
  gan: Kumar, Arun, et al.
  Cyhoeddwyd: (2007)
• 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)