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

SPG4 founder effect in French Canadians with hereditary spastic paraplegia.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques - 1 May 2007

Meijer Inge A, Dupré Nicolas, Brais Bernard, Cossette Patrick, St-Onge Judith, Rioux Marie-France, Benard Melanie, Rouleau Guy A

Abstract excerpt

BACKGROUND: The most common cause of autosomal dominant Hereditary Spastic Paraplegia (HSP) is mutations in the SPG4 gene. We have previously identified novel SPG4 mutations in a collection of North American families including the c.G1801A mutation present in two families from Quebec. The aim of...

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 Founder Effect
Share to France

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Quebec

Share to Spastic Paraplegia, Hereditary

Share to Spastin

Share to White People

Source

Identifiers

PMID: 17598600
DOI: 10.1017/s0317167100006065

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17598600-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SPG4 founder effect in French Canadians with hereditary spastic paraplegia.PMID 17598600Read ↗

Genetic, structural and clinical analysis of spastic paraplegia 4.Semantic proximity Read ↗

Clinical and genetic study of hereditary spastic paraplegia in CanadaSemantic proximity Read ↗

Genetic, structural and clinical analysis of spastic paraplegia 4Semantic proximity Read ↗

Clinical and molecular characterization of hereditary spastic paraplegia in a spanish Southern region.Semantic proximity Read ↗

Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.Semantic proximity Read ↗

Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia.Semantic proximity Read ↗

A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.Semantic proximity Read ↗

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

A SPAST gene-related hereditary spastic paraplegia type 4 family: Identification by a novel mutationSemantic proximity Read ↗

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

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

Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic ParaplegiaSemantic proximity Read ↗

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