Secondary C1q Deficiency in Activated PI3Kd Syndrome Type 2. (2019)
Attributed to:
UK Infrastructure for Large-scale Clinical Genomics Research
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.3389/fimmu.2019.02589
PubMed Identifier: 31781101
Publication URI: http://europepmc.org/abstract/MED/31781101
Type: Journal Article/Review
Volume: 10
Parent Publication: Frontiers in immunology
ISSN: 1664-3224