CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Molecular mechanism of a mild phenotype in coagulation factor XIII deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA
Authors
Haramura G
Hämäläinen E
+7 more
Laiho E
Mikkola H
Muszbek L
Palotie A
Peltonen L
Salmi T
Syrjälä M
Publication date
1 January 1997
Publisher
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Julkari
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:www.julkari.fi:10024/85784
Last time updated on 23/07/2013
