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Article

A novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia.

Chinese medical journal - 1 Jan 2014

Wang Xianling, Yang Yanhui, Wang Xiangbo, Li Cunjiang, Jia Jianping

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PMID: 24824269

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A novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia.PMID 24824269Read ↗

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Pure adult-onset spastic paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene.Semantic proximity Read ↗

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Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegiaSemantic proximity Read ↗

Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominant.Semantic proximity Read ↗

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Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case reportSemantic proximity Read ↗

Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.Semantic proximity Read ↗

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