Novel PITX2 Mutations including a Mutation Causing an Unusual Ophthalmic Phenotype of Axenfeld-Rieger Syndrome

<div>Detection of novel PITX2 mutations by heteroduplex-SSCP analysis. The plus sign (+) indicates samples with heterozygous variation, and the minus sign (−) indicates normal controls.</div>

Journal of Ophthalmology

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Figure 2: Novel PITX2 Mutations including a Mutation Causing an Unusual Ophthalmic Phenotype of Axenfeld-Rieger Syndrome 