MeSH Browser

MeSH Supplementary: miniagrin protein, mouse
Unique ID: C507258
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C507258
Registry Numbers: 0
Heading Mapped to: *Agrin
Frequency: 3
Note: a miniature version of agrin, can functionally compensates for laminin-alpha2 deficiency in the murine models of Congenital muscular dystrophy; GenBank AY914875
Source: Proc Natl Acad Sci U S A 2005 Aug 23;102(34):11999-2004
Date of Entry: 2006/01/23
Revision Date: 1955/01/01

miniagrin protein, mouse MeSH Supplementary Concept Data 2025