Figure 3.

Sequence analysis of a single base pair deletion mutation in BSCL2 gene (c.636delC). (a) DNA sequencing of exon 5 in an affected individual IV-1 (b) parent or carrier III-1 (c) unaffected or normal individual.

Rahman et al. Diagnostic Pathology 2013 8:78   doi:10.1186/1746-1596-8-78
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