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Article

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

27 Oct 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15517445
DOI: 10.1007/s10048-004-0191-2

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Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3APMID 15517445Read ↗

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Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.Semantic proximity Read ↗

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

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

Very early onset and severe complicated phenotype caused by a new spastic paraplegia 3A gene mutation.Semantic proximity Read ↗

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Hereditary spastic paraplegia associated with axonal neuropathy: a novel mutation of SPG3A in a large family.Semantic proximity Read ↗

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

Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.Semantic proximity Read ↗

The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia.Semantic proximity Read ↗

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