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. 2015 Oct 2;5:26–32. doi: 10.1016/j.ymgmr.2015.09.005

Fig. 2.

Fig. 2

Sequencing analysis in Case 15.

Case 15 had two pairs of heterozygous deletions (c.968_969 del TC) and substitutions (c.1813G > C) in the CPT2 gene. The father had a heterozygous deletion (c.968_969 del TC) while the mother had a heterozygous substitution (c.1813G > C).