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  • Tesi, B (author)

Gain-of-function SAMD9L mutations cause a syndrome with cytopenia, myelodysplastic syndrome, immunodeficiency and neurological disease

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:142061874
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:142061874URI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:vet swepub-contenttype
  • Subject category:kon swepub-publicationtype

Added entries (persons, corporate bodies, meetings, titles ...)

  • Davidsson, J (author)
  • Voss, M (author)
  • Rahikkala, E (author)
  • Holmes, T (author)
  • Chiang, S (author)
  • Komulainen-Ebrahim, J (author)
  • Gorcenco, S (author)
  • Nilsson, AR (author)
  • Ripperger, T (author)
  • Kokkonen, H (author)
  • Bryder, D (author)
  • Fioretos, T (author)
  • Henter, J (author)
  • Mottonen, M (author)
  • Niinimaki, R (author)
  • Nilsson, L (author)
  • Pronk, CJ (author)
  • Puschmann, A (author)
  • Qian, H (author)
  • Uusimaa, J (author)
  • Moilanen, J (author)
  • Tedgard, U (author)
  • Cammenga, J (author)
  • Bryceson, YT (author)

Related titles

  • In:EUROPEAN JOURNAL OF HUMAN GENETICS26, s. 315-3161018-4813

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