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Compound heterozygous mutations in the SLC4A11 gene associated with congenital hereditary endothelial dystrophy in a Chinese family.

Min LiuJia-Li XiaHong YangLing Yu
Published in: Ophthalmic genetics (2022)
gene in a Chinese family.
Keyphrases
  • early onset
  • copy number
  • genome wide
  • genome wide identification
  • endothelial cells
  • gene expression
  • dna methylation
  • genome wide analysis