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. Author manuscript; available in PMC: 2024 Oct 1.
Published in final edited form as: Clin Genet. 2024 Jun 11;106(4):505–511. doi: 10.1111/cge.14573

Figure 1. Clinical findings and family pedigrees for patients 1-3.

Figure 1

(A) Optos pseudocolour fundus photographs (a-f), Optos fundus autofluorescence (g-l) and Spectralis optical coherence tomography (OCT) images (m-r) for patients 1-3 with biallelic SUMF1 variants and retinal dystrophy (B) Family pedigrees showing genotypes and familial segregation where available.