A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy

<table>Pedigree and haplotype analysis for the XPV families (the disease haplotype is indicated by shading) and clinical photograph of each affected patient.</table>

BioMed Research International

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Figure 1

Figure 1: A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy 