Figure 1
From: Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD)
Characteristics of three new variants detected in PCD patients. a. Results of the SSCP analysis revealing different migration patterns, and pedigrees of the families where new mutations/SNPs were identified. New mutations (in patients 537, in his father 538, and in patients 507 and 336) are underlined. "?" denotes unknown mutation; the carrier status is indicated by a dot in the pedigree symbols. b. Chromatograms of the new sequence variants.