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Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

  • MJ Blok
  • , L Spruijt
  • , IFM Coo
  • , Kees Schoonderwoerd
  • , A Hendrickx
  • , HJ Smeets

Research output: Contribution to journalArticleAcademicpeer-review

64 Citations (Scopus)
Original languageUndefined/Unknown
JournalJournal of Medical Genetics
Volume44
Issue number4
Publication statusPublished - 2007

Research programs

  • EMC MGC-02-96-01
  • EMC MM-04-44-02

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