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Approximately half the cases of classical congenital muscular dystrophy (CMD) have a pronounced deficiency or absence of the laminin α2 chain of laminin-2 (merosin). This is caused by mutations in the LAMA2 gene that codes for laminin α2, and all informative cases so far studied show linkage to the appropriate region on chromosome 6q. Most CMD patients with a deficiency of laminin α2 have a severe...
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