Laminin subunit alpha-1
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Laminin subunit alpha-1 is a protein that in humans is encoded by the LAMA1 gene.[5][6]
External IDsOMIM: 150320; MGI: 99892; HomoloGene: 21146; GeneCards: LAMA1; OMA:LAMA1 - orthologs
Interactions
Role in pathology
Mutations of the LAMA1 gene cause the Poretti–Boltshauser syndrome.