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Article

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

Movement disorders : official journal of the Movement Disorder Society - 30 Apr 2008

Zhang Shu-Shan, Chen Qin, Chen Xue-Ping, Wang Jian-Gang, Burgunder Jean-Marc, Shang Hui-Fang, Burgunder Jean-Marc, Yang Yuan

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Share to Consanguinity
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Share to Gait Disorders, Neurologic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18361476
DOI: 10.1002/mds.21942

Genes

SPG11

Provenance

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Related research

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Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.PMID 18361476Read ↗

Novel SPG11 Mutation in Hereditary Spastic Paraplegia with Thin Corpus Callosum.Semantic proximity Read ↗

Hereditary spastic paraplegia with a thin corpus callosum due to SPG11 mutation.Semantic proximity Read ↗

Novel mutations c. [453dupA] + [663G > A] of the SPG11 gene associated with hereditary spastic paraplegia with a thin corpus callosum.Semantic proximity Read ↗

Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation.Semantic proximity Read ↗

Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation.Semantic proximity Read ↗

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

Novel SPG 11 Mutations in Hereditary Spastic Paraplegia With Thin Corpus Callosum in a Chinese Family.Semantic proximity Read ↗

Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

A case report of SPG11 mutations in a Chinese ARHSP-TCC family.Semantic proximity Read ↗

Novel SPG11 mutations in Chinese families with hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

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