Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: expanding the phenotypic spectrum of Rab27A mutations in humans. [electronic resource]

By: Contributor(s): Producer: 20030908Description: 329-33 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 116A
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Publication Type: Case Reports; Journal Article

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