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Figure 2 | BMC Medical Genetics

Figure 2

From: Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population

Figure 2

Mutation in the RP1 gene by A deletions. Pedigree, DGGE and direct sequencing of Spanish families showing K705fsX712 (A) and K722fsX737 (B) in the RP1 gene. Affected individuals, asymptomatic carriers and non-carriers of the mutation are represented by solid symbols, symbols with an internal dot and open symbols, respectively.

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BMC Medical Genetics

ISSN: 1471-2350

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