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

<div>Fundus photograph and fundus autofluorescence of the studied individuals. (a), (b), and (c) indicate fundus photographs in II: 3 (mother), II: 4 (father), and III: 1 (proband), respectively. (d) Fundus autofluorescence in III: 1 (proband), showing tigroid or tessellated features and conus pattern of retina.</div>

BioMed Research International

fig2

Figure 2

Figure 2: Identification of a Novel Heterozygous Missense Mutation in the <i>CACNA1F</i> Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing 

Figure 2 | Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing 