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The spectrum of SDHD mutations in Russian patients with head and neck paraganglioma.

Marina V ShulskayaMaria I ShadrinaNatalia A BakilinaSvetlana V ZolotovaPetr A Slominsky
Published in: The International journal of neuroscience (2018)
We found that mutations in the SDHD gene were less common in Russian patients compared with the majority of European populations. It was shown that the p.His102Arg mutation is a major mutation in Russia. We confirmed the previous suggestion that a bilateral localization of the tumor and the carotid type represent a marker of the genetically determined form of HNPGL.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • peritoneal dialysis
  • prognostic factors
  • patient reported outcomes