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LAMA2 - laminin subunit alpha 2
- Synonym(s) : congenital muscular dystrophy, merosin
- Previous symbols and names : LAMM, laminin, alpha 2
- Type : gene with protein product
- Chromosomal location : 6q22.33
- OMIM: 156225
- HGNC: 6482
- UniProtKB: P24043
- Genatlas: LAMA2
- GenCC: LAMA2
- Ensembl: ENSG00000196569
- IUPHAR-DB: -
- Reactome: P24043
- LOVD: LAMA2
Diseases list
- Disease-causing germline mutation(s) in Laminin subunit alpha 2-related congenital muscular dystrophy
ORPHA:258 
: AssessedAdditional information
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