Case Reports in Genetics / 2014 / Article / Fig 2

Case Report

Rhabdomyolysis and Cardiomyopathy in a 20-Year-Old Patient with CPT II Deficiency

Figure 2

Sequencing analysis demonstrating the detection of TCG > TTG or S113L mutation in exon 3 of the CPT II gene (a: patient; b: mother of the patient; c: normal control).
496410.fig.002a
(a)
496410.fig.002b
(b)
496410.fig.002c
(c)

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