Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing

<div>OCT and ERG images of the III: 1. The OCT images showed atrophy of the retina at macula fovea and losing of the fovea ((a), (b), and (c)). Full-field ERG characteristics in right eye ((d), (e), (f), (g), (h), and (i)).</div>

BioMed Research International

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Figure 3: Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing

Figure 3 | Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing 