Congenital Muscular Dystrophy Type1A MLPA

TEST CODE MG06300
TEST NAME Congenital Muscular Dystrophy Type1A MLPA
RELATED GENE LAMA2
SYNONYMOUS LAMA2
OMIM 607855
HEREDITY Autosomal Recessive
CLINICAL AREA Congenital Muscular Dystrophy Type 1A is an Autosomal Recessively inherited disease. Mutations in the LAMA2 gene have been associated with the disease. This test screens for deletion/duplication type mutations in the disease-related gene using the MLPA method.
METHOD MLPA
SAMPLE TYPE Blood with EDTA
QUANTITY 3 ml
TAT 40 DAYS

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