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Association of central serous chorioretinopathy with single nucleotide polymorphisms in complement factor H gene in Iranian population.

Reza KarkhanehMohsen ToufighiAkbar AmirfiroozyAliasghar Ahmad-RajiOveis AhmadzadehAlborz MahdaviMorteza Naderan
Published in: Eye (London, England) (2021)
The rs3753394 polymorphism is probably associated with CSCR in Persian ethnicity. Further studies are required to validate the implications of this finding in clinical practice.
Keyphrases
  • clinical practice
  • high grade
  • copy number
  • genome wide
  • case control
  • genome wide identification
  • gene expression