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

Podobne zapisy

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  od: Paliwal, Preeti, i wsp.
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  od: Paliwal, Preeti, i wsp.
  Wydane: (2010)
• Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
  od: Kumawat, Babu Lal, i wsp.
  Wydane: (2016)
• Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients with Fuchs Endothelial Corneal Dystrophy
  od: Okumura, Naoki, i wsp.
  Wydane: (2019)