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Heterozygous congenital Factor VII deficiency with the 9729de14 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male

Academic Article
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Overview

authors

  • Cramer, T. J.
  • Anderson, K.
  • Navaz, K.
  • Brown, J. M.
  • Mosnier, Laurent
  • von Drygalski, Annette

publication date

  • March 2016

journal

  • Blood Cells Molecules and Diseases  Journal

subject areas

  • Base Sequence
  • Bone Transplantation
  • Cerebral Hemorrhage
  • DNA Mutational Analysis
  • Decompressive Craniectomy
  • Epidural Abscess
  • Factor VII
  • Factor VII Deficiency
  • Factor VIIa
  • Gene Expression
  • Heterozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Recombinant Proteins
  • Sequence Deletion
  • Young Adult
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Research

keywords

  • EPCR
  • Factor VII deficiency
  • Recombinant Factor VII
  • Spontaneous intracranial hemorrhage
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Identity

PubMed Central ID

  • PMC4874642

International Standard Serial Number (ISSN)

  • 1079-9796

Digital Object Identifier (DOI)

  • 10.1016/j.bcmd.2015.11.004

PubMed ID

  • 26852649
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Additional Document Info

start page

  • 8

end page

  • 12

volume

  • 57

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