Whole-genome sequencing of patients with rare diseases in a national health system. (2020)
Attributed to:
ISCF HDRUK DIH Sprint Exemplar: Cloud-based integration of phenotype and genotype data for rare disease research
funded by
ISCF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41586-020-2434-2
PubMed Identifier: 32581362
Publication URI: http://europepmc.org/abstract/MED/32581362
Type: Journal Article/Review
Volume: 583
Parent Publication: Nature
Issue: 7814
ISSN: 0028-0836