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Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome.

AuthorsAnne Rensing-Ehl, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, Myriam Ricarda Lorenz, Benedicte Neven, Ilka Fuchs, Ulrich Salzer, Carsten Speckmann, Anne Strauss, Eberhard Maaβ, Benedicte Collet, Anselm Enders, Remi Favier, Marie Christine Alessi, Frederic Rieux-Laucat, Barbara Zieger, Klaus Schwarz, Stephan Ehl
JournalBlood (Blood) Vol. 126 Issue 16 Pg. 1967-9 (Oct 15 2015) ISSN: 1528-0020 [Electronic] United States
PMID26472737 (Publication Type: Case Reports, Clinical Trial, Letter, Research Support, Non-U.S. Gov't)
Chemical References
  • Blood Proteins
  • FAS protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • NBEAL2 protein, human
  • Nerve Tissue Proteins
  • PLXNB1 protein, human
  • Receptors, Cell Surface
  • fas Receptor
Topics
  • Autoimmune Lymphoproliferative Syndrome (diagnosis, genetics, metabolism, pathology)
  • Blood Proteins (genetics, metabolism)
  • Child, Preschool
  • Fas Ligand Protein (genetics, metabolism)
  • Female
  • Gray Platelet Syndrome (diagnosis, genetics, metabolism, pathology)
  • Humans
  • Infant
  • Male
  • Nerve Tissue Proteins (genetics, metabolism)
  • Receptors, Cell Surface (genetics, metabolism)
  • fas Receptor (genetics, metabolism)

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