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Fig. 1 | BMC Ophthalmology

Fig. 1

From: A novel variant in PAX6 as the cause of aniridia in a Chinese family

Fig. 1

Identification of the heterozygous mutation c.619A > T in PAX6 in a Chinese family with aniridia. a Pedigree of the family. Squares indicated males and circles indicated females. Empty symbols and filled symbols represented the normal and affected individuals, respectively. Wt: wild-type and Mt: mutation. b Sequence chromatograms showing the PAX6 c.619A > T mutation identified in this study. The arrows indicated the site of the mutation

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