CORE
đșđŠÂ
 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
Compound heterozygous <em>RMND1 </em>gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: A case report
Authors
Blakely EL
Colmenero I
+7Â more
Gupta A
He L
McFarland R
Milford DV
Ragge NK
Taylor RW
Vogt J
Publication date
27 June 2016
Publisher
'Springer Science and Business Media LLC'
Abstract
Abstract is not available.
Similar works
Full text
Open in the Core reader
Download PDF
Available Versions
Newcastle University E-Prints
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:eprints.ncl.ac.uk:235887
Last time updated on 30/05/2021