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 language | English (US) |
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Pages (from-to) | 1215-1216 |
Number of pages | 2 |
Journal | Blood |
Volume | 124 |
Issue number | 8 |
DOIs |
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State | Published - Aug 21 2014 |
ASJC Scopus subject areas
- Biochemistry
- Immunology
- Hematology
- Cell Biology