MeSH Browser

MeSH Supplementary: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Unique ID: C564317
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564317
Registry Number: 0
Heading Mapped to: Muscular Dystrophies / *congenital
Frequency: 1
Note: mutation in laminin alpha-2 (LAMA2)
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency MeSH Supplementary Concept Data 2024