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Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study. (2020)

First Author: Borghesi A

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