VKORC1 ER mislocalization causes rare disease

Research output: Contribution to journalArticle

2 Citations (Scopus)

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

Fingerprint

Vitamin K Epoxide Reductases
Blood Coagulation Factors
Vitamin K
Rare Diseases
Endoplasmic Reticulum
Blood

ASJC Scopus subject areas

  • Hematology
  • Biochemistry
  • Cell Biology
  • Immunology

Cite this

VKORC1 ER mislocalization causes rare disease. / Van Horn, Wade.

In: Blood, Vol. 124, No. 8, 21.08.2014, p. 1215-1216.

Research output: Contribution to journalArticle

Van Horn, Wade. / VKORC1 ER mislocalization causes rare disease. In: Blood. 2014 ; Vol. 124, No. 8. pp. 1215-1216.
@article{fc4b233a9ea145dd865903fe127b25a2,
title = "VKORC1 ER mislocalization causes rare disease",
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).",
author = "{Van Horn}, Wade",
year = "2014",
month = "8",
day = "21",
doi = "10.1182/blood-2014-07-586032",
language = "English (US)",
volume = "124",
pages = "1215--1216",
journal = "Blood",
issn = "0006-4971",
publisher = "American Society of Hematology",
number = "8",

}

TY - JOUR

T1 - VKORC1 ER mislocalization causes rare disease

AU - Van Horn, Wade

PY - 2014/8/21

Y1 - 2014/8/21

N2 - 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).

AB - 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).

UR - http://www.scopus.com/inward/record.url?scp=84907337113&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84907337113&partnerID=8YFLogxK

U2 - 10.1182/blood-2014-07-586032

DO - 10.1182/blood-2014-07-586032

M3 - Article

C2 - 25147380

AN - SCOPUS:84907337113

VL - 124

SP - 1215

EP - 1216

JO - Blood

JF - Blood

SN - 0006-4971

IS - 8

ER -