Reply: Expanding the clinical and genetic spectrum of PCYT2-related disorders.

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)1-2
Number of pages2
JournalBrain : a journal of neurology
Volume143
Issue number9
DOIs
Publication statusPublished - 1 Sept 2020

Keywords

  • Humans
  • Mutation/genetics
  • RNA Nucleotidyltransferases/genetics
  • Spastic Paraplegia, Hereditary

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