VKORC1 ER mislocalization causes rare disease

Research output: Contribution to journalComment/debate

2 Scopus citations

Abstract

In this issue of Blood, Czogalla et al identify that the rare heritable hemorrhaging disease, vitamin K-dependent clotting factor deficiency type 2 (VKCFD2), is caused by mislocalization of vitamin K epoxide reductase (VKORC1) in the endoplasmic reticulum (ER).

Original languageEnglish (US)
Pages (from-to)1215-1216
Number of pages2
JournalBlood
Volume124
Issue number8
DOIs
StatePublished - Aug 21 2014

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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