Whole-genome sequencing of a sporadic primary immunodeficiency cohort. (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/s41586-020-2265-1
PubMed Identifier: 32499645
Publication URI: http://europepmc.org/abstract/MED/32499645
Type: Journal Article/Review
Volume: 583
Parent Publication: Nature
Issue: 7814
ISSN: 0028-0836