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

HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier.

Neurology - 6 May 2008

Hewamadduma C A A, Kirby J, Kershaw C, Martindale J, Dalton A, McDermott C J, Shaw P J

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 Chaperonin 60
Share to Chromosome Disorders
Share to Genes, Dominant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Genetic Testing

Share to Spastic Paraplegia, Hereditary

Share to Spastin

Source

Identifiers

PMID: 18458233
DOI: 10.1212/01.wnl.0000311395.31081.70

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier.PMID 18458233Read ↗

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.Semantic proximity Read ↗

Hereditary spastic paraplegia: Genetic heterogeneity and common pathways.Semantic proximity Read ↗

An Update on the Hereditary Spastic Paraplegias: New Genes and New Disease ModelsSemantic proximity Read ↗

The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment.Semantic proximity Read ↗

Molecular aspects of hereditary spastic paraplegia.Semantic proximity Read ↗

Hereditary spastic paraplegia from 1880 to 2017: an historical reviewSemantic proximity Read ↗

Current insights into familial spastic paraparesis: new advances in an old disease.Semantic proximity Read ↗

Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1.Semantic proximity Read ↗

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

Hereditary spastic paraplegia: clinical principles and genetic advances.Semantic proximity Read ↗

Two novel truncating variants in UBAP1 are responsible for hereditary spastic paraplegia.Semantic proximity Read ↗

Perspectives on the Genomics of HSP Beyond Mendelian InheritanceSemantic proximity Read ↗

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