MeSH Browser

MeSH Supplementary: laminin alpha 2
Unique ID: C102645
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C102645
Entry Term(s): LAMA2 protein, human; LAMM protein, human; Lama2 protein, mouse; Laminin M chain protein, human; laminin, alpha 2 (merosin, congenital muscular dystrophy) protein, human; laminin, alpha 2 protein, mouse; merosin protein, mouse
Registry Numbers: 0
Heading Mapped to: *Laminin
Frequency: 375
Note: deficiency is associated with muscular dystrophy and demyelinating neuropathy; has been sequenced
Source: FEBS Lett 1996 Oct 28;396(1):37-42
Date of Entry: 1997/01/08
Revision Date: 2006/04/24

laminin alpha 2 MeSH Supplementary Concept Data 2025