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Fig. 2 | BMC Medical Genomics

Fig. 2

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

Fig. 2

NDP c.124C > A hemizygous mutation and the fundus avascular area of the FEVR2 patient in Family 18. In part a, fundus examination of the one-year-old patient showed an avascular area in both eyes. The temporal side of the blood vessel arch in the right eye fundus showed the epiretinal membrane and macular traction. Part b, NDP c.124C > A mutation of the mother and the child, respectively

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BMC Medical Genomics

ISSN: 1755-8794

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