Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. (2021)
Attributed to:
Disease mechanisms and therapy for inherited disorders of the neuromuscular synapse.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-021-00859-0
PubMed Identifier: 34075208
Publication URI: http://europepmc.org/abstract/MED/34075208
Type: Journal Article/Review
Volume: 29
Parent Publication: European journal of human genetics : EJHG
Issue: 9
ISSN: 1018-4813