Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations.

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • H Shima - (Author)
  • K Koehler - , Department of Paediatrics (Author)
  • Y Nomura - (Author)
  • K Sugimoto - (Author)
  • A Satoh - (Author)
  • T Ogata - (Author)
  • M Fukami - (Author)
  • Ramona Jühlen - (Author)
  • M Schuelke - (Author)
  • K Mohnike - (Author)
  • A Huebner - , Department of Paediatrics (Author)
  • S Narumi - (Author)

Details

Original languageUndefined
JournalJournal of medical genetics
Publication statusPublished - Nov 2017
Peer-reviewedYes

External IDs

PubMed 29175836
Scopus 85043346589

Keywords