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Fig. 1 | BMC Ophthalmology

Fig. 1

From: Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family

Fig. 1

Clinical evaluation of a Chinese pedigree with autosomal dominant congenital cataract. a Pedigree of a six-generation Chinese family with autosomal dominant congenital cataracts. The arrow indicates the proband. Squares and circles symbolize males and females, respectively. Black and white denote the status of family members affected or unaffected, respectively, by congenital cataract. b Photo was taken with a surgical microscope

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BMC Ophthalmology

ISSN: 1471-2415

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