Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson.

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Description

Keratoconus is a common ocular disorder that causes progressive corneal thinning and is the leading indication for corneal transplantation. Central corneal thickness (CCT) is a highly heritable characteristic that is associated with keratoconus. In this two-stage genome-wide association study (GWAS) of CCT, we identified a locus for CCT, namely STON2 rs2371597 (P = 2.32 × 10

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Details 詳細情報について

  • CRID
    1871710641494632320
  • HANDLE
    2433/253548
  • ISSN
    23993642
  • PubMed
    32737415
  • Data Source
    • OpenAIRE

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