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. Author manuscript; available in PMC: 2013 Oct 19.
Published in final edited form as: Arch Ophthalmol. 2012 Oct;130(10):1301–1308. doi: 10.1001/archophthalmol.2012.1906

Figure 1.

Figure 1

Pedigree and electropherogram of the family studied. A, Pedigree with autosomal recessive retinal degeneration segregates with the c.1381 C>T CDHR1 mutation. Squares indicate males; circles, females; shaded symbols, retinal degeneration; double lines, consanguinity; and slash marks, individuals who had died. B, Electropherograms with the sequence of the CDHR1 gene encompassing the c.1381 C/T region showing the homozygous c.1381 C>T change identified in the affected siblings, the sequence of an unaffected family member with the c.1381 C>T change in the heterozygous state, and the wild-type sequence at the c.1381 nucleotide of the CDHR1 gene.