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Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family.

Gonca Kilic YildirimCoskun YararBerna Seker YilmazSerdar Ceylaner
Published in: Journal of pediatric endocrinology & metabolism : JPEM (2021)
When combined with the filipin staining and the patients' clinical outcomes, this mutation is likely to be deleterious. Moreover, cDNA sequencing supports the pathogenicity of this novel variant.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • peritoneal dialysis
  • escherichia coli
  • patient reported outcomes