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A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.

Pooja SharmaAkhilesh K SonakarVinay GoelAjay GargAchal Kumar SrivastavaMohammed Faruq
Published in: Movement disorders clinical practice (2022)
These cases highlight the probabilistic interactive outcome of two unrelated genetic events towards a converging phenotype.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • early onset
  • peritoneal dialysis
  • gene expression
  • patient reported outcomes
  • dna methylation