The S349T mutation of SQSTM1 links Keap1/Nrf2 signalling to Paget's disease of bone. (2013)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.bone.2012.10.023
PubMed Identifier: 23117207
Publication URI: http://europepmc.org/abstract/MED/23117207
Type: Journal Article/Review
Volume: 52
Parent Publication: Bone
Issue: 2
ISSN: 1873-2763