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Novel variants in Turkish patients with glycogen storage disease.

Nafiye Emel ÇakarAlper GezdiriciHanım Şeyma TopuzHasan Önal
Published in: Pediatrics international : official journal of the Japan Pediatric Society (2020)
We determined the gene mutations specific to cohorts in our cases with GSD. The novel pathogenic, likely pathogenic, and VUS changes identified will contribute to the relationship between the patients' clinical and laboratory findings.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • prognostic factors
  • peritoneal dialysis
  • copy number
  • gene expression
  • dna methylation
  • genome wide