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Laminin subunit alpha-1
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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Laminin subunit alpha-1 is a protein that in humans is encoded by the LAMA1 gene.[5][6]
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Interactions
Laminin, alpha 1 has been shown to interact with FBLN2.[7][8]
Role in pathology
Mutations of the LAMA1 gene cause the Poretti–Boltshauser syndrome.
References
Further reading
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