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Gout inheritance in an extended Chinese family analyzed by whole-exome sequencing: A case-report.

Peiqing YangXuenan PiTony N MarionJing WangGang WangYan XieDan XieYi Liu
Published in: Medicine (2020)
In the case of this family, the GWAS identified gout and UC-related nucleotide sequence variants may increase the risk of developing gout, but penetrance was not complete. The rare sequence variants in low-density lipoprotein receptor-related protein 1 (LRP1) and oncoprotein induced transcript 3 (OIT3) may have contributed to inheritance of gout within the 5 generations of family members in this study.
Keyphrases
  • uric acid
  • low density lipoprotein
  • copy number
  • mitochondrial dna
  • metabolic syndrome
  • high glucose
  • diabetic rats
  • drug induced
  • oxidative stress
  • dna methylation
  • endothelial cells
  • genome wide
  • binding protein