Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report
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Congenital muscular dystrophies (CMD) are a heterogeneous group of disorders caused by mutations in musculoskeletal proteins. The most common type of CMD in Europe is Merosin-deficient CMD caused by mutations in laminin-α2 protein. Very few studies reported p... ...
