Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study. (2020)
Attributed to:
The genetic basis of invasive meningococcal disease
funded by
UKRI FLF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/cid/ciaa290
PubMed Identifier: 32185379
Publication URI: http://europepmc.org/abstract/MED/32185379
Type: Journal Article/Review
Volume: 71
Parent Publication: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Issue: 10
ISSN: 1058-4838