Additional file 3: of Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies

  • Chantal H. Kerkhofs (Contributor)
  • Riikka Keski-Filppula (Contributor)
  • Wendy A. G. van Zelst-Stams (Contributor)
  • Jayne Y. Hehir-Kwa (Contributor)
  • Alaa B. Alsaad (Contributor)
  • Arjen R. Mensenkamp (Contributor)
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  • Sarah Hortillosa (Contributor)
  • Evelien Zonneveld-Huijssoon (Contributor)
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  • Chantal P. Bleeker-Rovers (Contributor)
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  • Tomasz Stokowy (Contributor)
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  • Joris A. Veltman (Contributor)
  • Eissa A. Faqeih (Contributor)
  • Stefan H Lelieveld (Contributor)
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  • Janneke H. M. Schuurs-Hoeijmakers (Contributor)
  • Mihai G. Netea (Contributor)
  • Gijs T. J. Van Well (Contributor)
  • Erica Gerkes (Contributor)
  • Maaike Vreeburg (Contributor)
  • Abdulrahman A. Al-Hussaini (Contributor)
  • Fahad AlManjomi (Contributor)
  • Murad K. Habazi (Contributor)
  • Jaap ten Oever (Contributor)
  • Abdulrahman A. Andijani (Contributor)
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  • Hadeel A. AlJubab (Contributor)
  • Peer Arts (Contributor)
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  • Badr Alsaleem (Contributor)
  • Marius A. MacKenzie (Contributor)
  • Hamza A. AlGhamdi (Contributor)
  • Anja Wagner (Contributor)
  • Frank L. van de Veerdonk (Contributor)
  • Judith Potjewijd (Contributor)
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  • Maartje van de Vorst (Contributor)
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  • Elanur Yilmaz (Contributor)
  • Anna Simon (Contributor)

    Dataset

    Description

    Table S3. Variants of unknown significance (class 3) and variants in TRAF3 identified in 17 patients suffering from primary immunodeficiencies. (XLSX 11 kb)
    Date made available17-Jun-2019
    PublisherUniversity of Groningen

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