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Figure 1 | BMC Medical Genetics

Figure 1

From: A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss

Figure 1

Pedigree of a six-generation Chinese Han family that harbors the 1555A > G mutation with aminoglycoside-induced and nonsyndronic hearing loss. Individuals with hearing loss are indicated by filled symbols. The arrow indicates the proband. All matrilineal relatives of this family were homoplasmic for the 1555A > G mutation except for subject II2 who was heteroplasmic.

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