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Fig. 3 | BMC Ophthalmology

Fig. 3

From: Identification of a novel RHO heterozygous nonsense mutation in a Chinese family with autosomal dominant retinitis pigmentosa

Fig. 3

Sanger sequencing of RHO and bioinformatics analysis of the mutation. A Sanger sequencing of RHO detected a c.1015A > T transversion in affected patients which caused the replacement of a wild-type Lysine with stop codon at codon 339. B Multiple-sequence alignments of RHO in various species showed codon 339 was located within a highly conserved region

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BMC Ophthalmology

ISSN: 1471-2415

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