Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

B. Garavaglia, V. Colamaria, F. Carrara, P. Tonin, M. Rimoldi, G. Uziel

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)301-303
Number of pages3
JournalJournal of Inherited Metabolic Disease
Issue number3
Publication statusPublished - May 1994

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Endocrinology

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