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Figure 3 | BMC Medical Genetics

Figure 3

From: A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

Figure 3

PEX6 protein levels evaluated by immunoblotting. Results from cultured fibroblasts obtained from ZS patients B1 and D2 (both homozygous for PEX6 c.802_815del) are shown along with two PEX6 null mutants, and a normal control. Genotypes for PEX6 null mutant 1: c.[499_500del]; [2095-10_21del] and PEX6 null mutant 2: c.[1314_1320del];[2472-2A > G]. The results from b-tubulin analysis are provided as loading control

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BMC Medical Genetics

ISSN: 1471-2350

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