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Figure 1 | BMC Medical Genetics

Figure 1

From: Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology

Figure 1

Pedigree of patient with ataxia and congenital cataracts. Four generations of the family of a proband with ataxia and congenital cataracts. Genotypes for the SETX mutation chr9:135,176,191, C > T and the OCRL mutation is chrX:128695181, G > A are shown for the proband and his parents. Several members of the maternal lineage were noted to have early onset cataracts.

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