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. Author manuscript; available in PMC: 2018 Mar 7.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):594–603. doi: 10.1167/iovs.16-21026

Figure 3.

Figure 3

(A) Pedigree of Family II included in this study. Arrows indicate proband. White square or circle = unaffected individual; black square or circle = affected individual; white circle with black segment = individual reported to have eye problems and short stature but not formal diagnosis; * = individual with eye abnormalities and/or short stature. (B) Family II shows chromatogram of PEX11B c.136C>T p.(Arg46Ter) homozygous variant in II.1 that is heterozygous in his mother (arrow indicates altered nucleotide).