Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1

Saved in:
Bibliographic Details
Published in:PloS one 2015-08, Vol.10 (8), p.e0136011-e0136011
Main Authors: Johnsrud, Irene, Kulseth, Mari Ann, Rødningen, Olaug Kristin, Landrø, Linn, Helsing, Per, Waage Nielsen, Erik, Heimdal, Ketil
Format: Article
Language:English
Subjects:
Angioedema
Complement component C1
Hospitals
Medical research
Mutation
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0136011