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Copy number variation analysis using next-generation sequencing identifies the CFHR 3/ CFHR 1 deletion in atypical hemolytic uremic syndrome: a case report.

Joonhong ParkHo-Young YhimKyung Pyo KangTae Won BaeYong Gon Cho
Published in: Hematology (Amsterdam, Netherlands) (2022)
genes in patients with suspected aHUS.
Keyphrases
  • copy number
  • genome wide
  • mitochondrial dna
  • dna methylation
  • case report
  • gene expression
  • genome wide identification