MeSH Browser

MeSH Supplementary: Fras1 protein, mouse
Unique ID: C482018
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C482018
Entry Term(s): Fraser syndrome 1 homolog (human) protein, mouse
Registry Numbers: 0
Heading Mapped to: *Extracellular Matrix Proteins
Frequency: 27
Note: mutations in gene are associated with Fraser syndrome; represents animal model of human disease; RefSeq NM_175473
Source: Nat Genet 2004 Feb;36(2):172-7
Indexing Information: Denys-Drash Syndrome
Date of Entry: 2004/02/27
Revision Date: 2005/08/10

Fras1 protein, mouse MeSH Supplementary Concept Data 2025