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Fig. 1 | BMC Ophthalmology

Fig. 1

From: X-linked dominant RPGR gene mutation in a familial Coats angiomatosis

Fig. 1

Pedigree of the family. a Black circle and squares indicate affected individuals. Black arrow indicates the proband who underwent NGS panel (III:1). Black lines at the top indicates available DNAs for segregation analysis (III:2, III:3 and II:2). b Sanger Sequencing Electropherograms showing on the top the proband (III:1) genotype of RPGR variant (black arrow) and below the wild-type (WT) genotype

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