Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Novel mutation in the SPAST gene in a patient with spastic paraparesis.

Journal of neurology - 1 Feb 2008

Vergouwen M D I, Sistermans E A, Baas F, Koelman J H, de Visser M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Triphosphatases
Share to Aged
Share to DNA
Share to Electromyography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Neuropsychological Tests

Share to Paraparesis, Spastic

Share to Spastin

Source

Identifiers

PMID: 18038174
DOI: 10.1007/s00415-007-0728-z

Genes

SPAST

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mutation in the SPAST gene in a patient with spastic paraparesis.PMID 18038174Read ↗

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

Case report on novel mutation in SPAST gene in Polish family with spastic paraplegia.Semantic proximity Read ↗

A novel missense mutation in SPAST causes hereditary spastic paraplegia in male members of a family: A case report.Semantic proximity Read ↗

[A novel mutation of SPAST gene in a hereditary spastic paraplegia type 4 family].Semantic proximity Read ↗

Novel genetic variant in hereditary spastic paraparesis.Semantic proximity Read ↗

Spastin gene mutation in Japanese with hereditary spastic paraplegia.Semantic proximity Read ↗

A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.Semantic proximity Read ↗

Identification of c.1495C > T mutation in SPAST gene in a family of Han Chinese with hereditary spastic paraplegia.Semantic proximity Read ↗

The rumpshaker mutation in spastic paraplegiaSemantic 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 ↗

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.