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Article

A case report of a woman with young onset cognitive impairment associated with hereditary spastic paraplegia due to a mutation in the SPAST gene.

Journal of the neurological sciences - 15 Aug 2016

Tisher Annya, Salardini Arash

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Share to Adenosine Triphosphatases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27423575
DOI: 10.1016/j.jns.2016.05.057

Genes

SPAST

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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A case report of a woman with young onset cognitive impairment associated with hereditary spastic paraplegia due to a mutation in the SPAST gene.PMID 27423575Read ↗

Association of Early-Onset Spasticity and Risk for Cognitive Impairment With Mutations at Amino Acid 499 in SPAST.Semantic proximity Read ↗

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Infantile-onset ascending spastic paraplegia phenotype associated with SPAST mutation.Semantic proximity Read ↗

Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.Semantic proximity Read ↗

Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males.Semantic proximity Read ↗

Novel mutation of the Spastin gene in familial spastic paraplegia.Semantic proximity Read ↗

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