Common Variable Immunodeficiency in a Carrier of the ADA2 R169Q Variant: Coincidence or Causality?

Details

Request a copyRequest a copy
Serval ID
serval:BIB_CB464CB7181B
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
UNIL/CHUV
Title
Common Variable Immunodeficiency in a Carrier of the ADA2 R169Q Variant: Coincidence or Causality?
Journal
Journal of clinical immunology
Author(s)
Moi L., Schnider C., Riccio O., Hershfield M.S., Candotti F.
ISSN
1573-2592 (Electronic)
ISSN-L
0271-9142
Publication state
Published
Issued date
07/2022
Peer-reviewed
Oui
Volume
42
Number
5
Pages
959-961
Language
english
Notes
Publication types: Case Reports ; Letter
Publication Status: ppublish
Keywords
Adenosine Deaminase/genetics, Common Variable Immunodeficiency/diagnosis, Common Variable Immunodeficiency/genetics, Humans, Intercellular Signaling Peptides and Proteins/genetics, Phenotype
OAI-PMH
oai:serval.unil.ch:BIB_CB464CB7181B
DOI
10.1007/s10875-022-01271-z
Pubmed
35449494
Web of science
000784608000002
Create date
03/05/2022 8:53
Last modification date
05/05/2023 6:58
Usage data