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Fig. 1 | Journal of Translational Medicine

Fig. 1

From: Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia

Fig. 1

Pedigrees and identified mutations. a Pedigrees of two families were demonstrated with CNGA3 genotypes was annotated to included family members. Probands are indicated by arrows. Circles females; squares males; filled symbols affected patients; empty symbols unaffected controls. b DNA sequencing profiles of the identified mutations (upper) and their wild-type form (under)

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Journal of Translational Medicine

ISSN: 1479-5876

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