Global ETD Search
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Showing 1 to 1 of 1 for “"LAMA2-CMD"”.
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The role of recombinant human laminin-111 in adhesion-signaling and glycosylation in laminin-⍺2 deficient muscle
LAMA2-related congenital muscular dystrophy (LAMA2-CMD) is a rare and severe neuromuscular disease characterized by progressive muscular degeneration. LAMA2-CMD is caused by mutations in LAMA2 which encodes for the laminin-α2 protein. Loss of laminin-α2 results in the absence of laminin-211/221, an …