Residues 155 and 348 contribute to the determination of P2X7 receptor function via distinct mechanisms revealed by single-nucleotide polymorphisms. (2011)
Attributed to:
a state of the art facility for the study of protein trafficking in vivo
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1074/jbc.m110.211284
PubMed Identifier: 21205829
Publication URI: http://europepmc.org/abstract/MED/21205829
Type: Journal Article/Review
Volume: 286
Parent Publication: The Journal of biological chemistry
Issue: 10
ISSN: 0021-9258