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Figure 3 | BMC Medical Genetics

Figure 3

From: Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation

Figure 3

Pedigrees of families carrying the m.1005T > C variant (continued). (A,B) Audiograms of the siblings (III: 3, 4) of a family carrying the heteroplasmic m.1005T > C (Figure 2C). (C) Predicted secondary structure of the 12S rRNA transcript with the m.1005T > C. To the right is shown an enlargement of the region of predicted secondary structures surrounding nucleotide position 1005.

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BMC Medical Genetics

ISSN: 1471-2350

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