A novel TSC2 mutation in a Chinese family with tuberous sclerosis complex.

The article discusses a study on Chinese family with multisystem disorder tuberous sclerosis complex (TSC). The study included mutation screening of the TSC1/TSC2 gene, extraction of genomic DNA, and primer designing for amplification of TSC1/TSC2 gene's whole exons and exon-intron boundaries, and polymerase chain reaction. Also mentions that the study showed autosomal dominant inheritance for the TSC.