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Figure 1 | BMC Medical Genetics

Figure 1

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

Figure 1

PEX6 founder mutation c.802_815del. Sanger sequencing traces are shown for patient D2 (homozygote), and his mother and father (heterozygotes). The reference sequence is shown at the bottom with the deleted sequence underlined (Ref Seq NM_000287.3). The arrow indicates the position of the 14-bp deletion. PEX6 exon 1 extends from nucleotides 1–882

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BMC Medical Genetics

ISSN: 1471-2350

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