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GRN mutation spectrum and genotype-phenotype correlation in Chinese dementia patients: data from PUMCH dementia cohort.

Caiyan LiuLiling DongJie WangJie LiXinying HuangDan LeiChenhui MaoShanshan ChuLongze ShaQi XuBin PengLiying CuiJing Gao
Published in: Journal of medical genetics (2024)
mutations.
Keyphrases
  • mild cognitive impairment
  • end stage renal disease
  • cognitive impairment
  • newly diagnosed
  • ejection fraction
  • chronic kidney disease
  • big data
  • patient reported outcomes
  • patient reported
  • deep learning