Figure 3
From: Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family
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.
