[Molecular medicine: pathobiochemistry as the key to personalized treatment of inherited diseases].

Johannes A. Mayr (First author), René Feichtinger (Co-author), Melanie Achleitner, K Brugger, K Kutsam, Johannes Spenger (Co-author), Johannes Koch (Co-author), P Hofbauer, Florian Lagler (Co-author), Wolfgang Sperl (Co-author), Daniel Weghuber (Co-author), Saskia Wortmann (Last author)

Research output: Contribution to journalOriginal Articlepeer-review

Original languageGerman
Pages (from-to)828-836
JournalMonatsschrift Kinderheilkunde
Volume169
Issue number9
DOIs
Publication statusPublished - 2021

Keywords

  • DEFICIENCY
  • SPECTRUM
  • TRANSPLANTATION
  • DEHYDROGENASE
  • MUTATIONS
  • DEFECTS

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