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Figure 1

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Figure 1

Pedigree of a consanguineous Moroccan family with three patients with Leigh syndrome. Black symbols indicate affected, white symbols unaffected subjects. The genotypes for the c.477A→C mutation in exon 5 of the C20orf7 gene are indicated below the tested individuals. The proband is indicated by an arrow.

Vol 61 Issue 4 Table of Contents
Journal of Medical Genetics: 61 (4)
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