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Fig. 7 | BMC Medical Genetics

Fig. 7

From: Identification of a novel TSC2 c.3610G > A, p.G1204R mutation contribute to aberrant splicing in a patient with classical tuberous sclerosis complex: a case report

Fig. 7

RNA analysis. a Electrophoresis for amplification of TSC2 cDNA in the proband and a normal person. b Sequencing chromatogram of TSC2 cDNA in the proband and a normal person. Upper panel, wild type; Middle panel, transcripts with missense mutation c.3610G > A; Lower panel, transcripts lacking exon 29. The asterisk indicated the position of mutation (c.3610G > A) of exon 29 in TSC2

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