Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature

Podobne zapisy

• Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11
  od: Kumar, Arun, i wsp.
  Wydane: (2007)
• SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy
  od: Patel, Sangita P., i wsp.
  Wydane: (2015)
• Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy
  od: Kapoor, Saketh, i wsp.
  Wydane: (2012)
• Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort
  od: Paliwal, Preeti, i wsp.
  Wydane: (2010)
• Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex
  od: Kapoor, Saketh, i wsp.
  Wydane: (2016)