| Literature DB >> 18523871 |
B Perbal1.
Abstract
A recent manuscript reported phenotypic alterations associated to the expression of a CCN3 protein deleted for the Von Willebrand type C repeat that is common to the various members of the CCN family of proteins. In this comment, the biological significance of these alterations is briefly discussed.Entities:
Year: 2008 PMID: 18523871 PMCID: PMC2443240 DOI: 10.1007/s12079-008-0020-8
Source DB: PubMed Journal: J Cell Commun Signal ISSN: 1873-9601 Impact factor: 5.782