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Fig. 1 | BMC Neurology

Fig. 1

From: An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions

Fig. 1

A Pedigree of the family. The proband (IV-5) had a homozygous variant of SPG11. The parents (III-3 and III-8) were cousins. B Electropherogram of SPG11 variants. A homozygous splice site variant of c.4162–2A > G was identified in the patient. A heterozygous variant at the same location was identified in the parents. The location of the variant is shown by the red arrow

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BMC Neurology

ISSN: 1471-2377

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