Fig. 1 | Genetics in Medicine

Fig. 1

From: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Fig. 1

Fundus and optical coherence tomography (OCT) imaging in patients with RAX2-associated ARRP. a–f Fundus images and (g–l) OCT images of patients I–VI (left eye) show features characteristic of retinitis pigmentosa as described in further detail in Table 1 and Supplementary File 2. Notable features include variable degrees of pigmentation and a general preservation of foveal structure.

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