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Fig. 3 | BMC Medical Genomics

Fig. 3

From: Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technology

Fig. 3

In Part a, P-VEP examination of the older sister with a binocular patchy visual field in Family 2 showed bilateral P100 wave latency delay with normal amplitude. F-ERG examination showed binocular light adaptation, moderately or severely decreased 30 Hz response amplitude, and moderately decreased other response amplitudes; a binocular dark response could not be induced, OPS wavelets could not be separated, other waves could be induced, and the amplitude decreased moderately. Part b shows the Sanger sequencing results of the mutated site

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