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Genetic confirmation that ependymoma can arise as part of multiple endocrine neoplasia type 1 (MEN1) syndrome

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References

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Authors and Affiliations

  1. Division of Neuropathology, Department of Pathology, University of California, San Francisco, 513 Parnassus Ave, Health Sciences West 451, San Francisco, CA, 94143, USA

    Areli K. Cuevas-Ocampo, Andrew W. Bollen, Benjamin Goode, Arie Perry & David A. Solomon

  2. Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany

    Kristian W. Pajtler, Lukas Chavez & Tanvi Sharma

  3. Department of Pediatric Oncology, Hematology and Immunology, University Hospital, Heidelberg, Germany

    Kristian W. Pajtler

  4. German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany

    Lukas Chavez & Andrey Korshunov

  5. Division of Gastroenterology, Department of Medicine, University of California, San Francisco, CA, USA

    Sun-Chuan Dai

  6. Department of Neurological Surgery, University of California, San Francisco, CA, USA

    Michael McDermott & Arie Perry

  7. Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany

    Andrey Korshunov

  8. Department of Neuropathology, University Hospital, Heidelberg, Germany

    Andrey Korshunov

  9. Clinical Cancer Genomics Laboratory, University of California, San Francisco, CA, USA

    David A. Solomon

Authors
  1. Areli K. Cuevas-Ocampo
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  2. Andrew W. Bollen
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  3. Benjamin Goode
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  4. Kristian W. Pajtler
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  5. Lukas Chavez
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  6. Tanvi Sharma
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  7. Sun-Chuan Dai
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  8. Michael McDermott
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  9. Arie Perry
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  10. Andrey Korshunov
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  11. David A. Solomon
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Corresponding author

Correspondence to David A. Solomon.

Additional information

This study was supported by NIH Director’s Early Independence Award (DP5 OD021403) to D.A.S.

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Cuevas-Ocampo, A.K., Bollen, A.W., Goode, B. et al. Genetic confirmation that ependymoma can arise as part of multiple endocrine neoplasia type 1 (MEN1) syndrome. Acta Neuropathol 133, 661–663 (2017). https://doi.org/10.1007/s00401-017-1689-7

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  • DOI: https://doi.org/10.1007/s00401-017-1689-7

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