Skip to main content
Figure 2 | BMC Medical Genetics

Figure 2

From: Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus

Figure 2

Phylogenetic network based on mtDNA D-loop sequences in 79 patients with epilepsy. Nodes represent patients. Inside the nodes, patients are identified by numbers 1-79. Outgroup is an African sequence [GenBank: AF346980]; CRS is the revised Cambridge Reference Sequence [GenBank: NC_012920]. Unless marked otherwise, mtDNA variants are transitions. Superscripts indicate transversions and novel mutations. @ = back mutation, * = heteroplasmic mutation.

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us