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Fig. 4 | BMC Medical Genetics

Fig. 4

From: Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case report

Fig. 4

Summary of the variants and amino acid alterations of ECHS1 gene related to Leigh syndrome. (A) The previously reported variants (below the bar with dashed lines) and the newly identified variants (above the bar with solid lines); (B) The previously reported amino acid alterations (below the bar with dashed lines) and the newly identified amino acid alterations (above the bar with solid lines)

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