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  • Molecular assay reagents intended to identify mutations in the tuberous sclerosis 1 (TSC1) gene, located at chromosome 9q34, which is implicated as a tumor suppressor. This inherited genetic mutation has been identified in patients with tuberous sclerosis type 1; it is also associated with focal cortical dysplasia of Taylor balloon cell subtype (epilepsy-associated) and lymphangiomyomatosis in females.
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