Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India

Những quyển sách tương tự

• Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort
  Bằng: Paliwal, Preeti, et al.
  Được phát hành: (2010)
• Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy
  Bằng: Paliwal, Preeti, et al.
  Được phát hành: (2010)
• TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies
  Bằng: Paliwal, Preeti, et al.
  Được phát hành: (2010)
• Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
  Bằng: Kumawat, Babu Lal, et al.
  Được phát hành: (2016)
• Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients with Fuchs Endothelial Corneal Dystrophy
  Bằng: Okumura, Naoki, et al.
  Được phát hành: (2019)