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Novel genetic variations in LAMA2 and SGCG genes. Sequencing of the LAMA2 gene revealed two novel intronic variations: a c.3174+22_23insAT insertion in intron 22 and a c.6085+12delA deletion in intron 42. Sequencing of SGCG gene revealed an A > C substitution at position +102 in the 3'UTR region.
