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PUBLICATIONS · 27182967

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.

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Bibliographic metadata only. No full-text article or abstract is reproduced. Absence of a captured notice is not confirmation that a publication is clear of corrections or retractions.

Journal
Nat Genet
Publication date
2016 Jul
First author
Narumi S

Publication notices

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true
has correction metadata
false
has expression of concern metadata
false
has retraction in link
false
pubmed marks article retracted
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pubmed marks retraction notice
false
relationships

    Authors and identifiers

    1. name
      Narumi S
      type
      Author
    2. name
      Amano N
      type
      Author
    3. name
      Ishii T
      type
      Author
    4. name
      Katsumata N
      type
      Author
    5. name
      Muroya K
      type
      Author
    6. name
      Adachi M
      type
      Author
    7. name
      Toyoshima K
      type
      Author
    8. name
      Tanaka Y
      type
      Author
    9. name
      Fukuzawa R
      type
      Author
    10. name
      Miyako K
      type
      Author
    11. name
      Kinjo S
      type
      Author
    12. name
      Ohga S
      type
      Author
    Complete bibliographic record and source provenance
    authors
    1. name
      Narumi S
      type
      Author
    2. name
      Amano N
      type
      Author
    3. name
      Ishii T
      type
      Author
    4. name
      Katsumata N
      type
      Author
    5. name
      Muroya K
      type
      Author
    6. name
      Adachi M
      type
      Author
    7. name
      Toyoshima K
      type
      Author
    8. name
      Tanaka Y
      type
      Author
    9. name
      Fukuzawa R
      type
      Author
    10. name
      Miyako K
      type
      Author
    11. name
      Kinjo S
      type
      Author
    12. name
      Ohga S
      type
      Author
    bibliography ids
    1. nci-bib-e8942a80013bd03823b475c7
    book metadata
    content sha256
    263a6101b0d47c861873b928891d17520403bce778e2553e74c88cc7561052db
    document type
    citation
    dois
    1. 10.1038/ng.3569
    electronic publication date
    display
    2016 May 16
    precision
    day
    year
    2016
    evidence scope
    bibliographic_metadata_only
    id
    pubmed:27182967
    immutable id
    pubmed:27182967@263a6101b0d47c861873b928891d17520403bce778e2553e74c88cc7561052db
    journal
    abbreviation
    Nat Genet
    issn electronic
    1546-1718
    issn print
    1061-4036
    issue
    7
    name
    Nature genetics
    nlm unique id
    9216904
    pages
    792-7
    volume
    48
    languages
    1. eng
    notices
    absence is not clearance
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    has correction metadata
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    has expression of concern metadata
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    has retraction in link
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      outcomes validated
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      pmid
      27182967
      provenance
      batch id
      fe5a46c92522c34737e8
      provider
      NCBI PubMed ESummary
      record sha256
      a83e4b7e0759b45a862bf7963b65a93dfb4030552f4dbe3b005cf0892bcdfdc9
      response sha256
      2c7bacd02d2ece3813daf1a0f92260c22884bd9268942fcca2088ab229bfb4d1
      retrieved at
      2026-09-09T23:47:17.939307+00:00
      publication date
      display
      2016 Jul
      precision
      month
      year
      2016
      publication types
      1. Journal Article
      record status
      PubMed - indexed for MEDLINE
      schema version
      1.0
      source url
      https://pubmed.ncbi.nlm.nih.gov/27182967/
      title
      SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.

      Preserved source evidence · Independent clinical review pending · Not medical advice