Fig. 1From: Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegiaChromatograms of 11 mutations identified in the present study. The upper chromatogram in each frame represents the reference sequence, and the lower one depicts the mutant sequence. The p.R112X in CYP7B1, p.S242 N in ALDH18A1, p.D597fs in GBA2, c.759 + 1G > A in CAPN1, and p.Q486XA in TP13A2 are homozygousBack to article page