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

Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene.

Neurology - 14 Aug 2007

Brugman F, Eymard-Pierre E, van den Berg L H, Wokke J H J, Gauthier-Barichard F, Boespflug-Tanguy O

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 Adolescent
Share to Age Factors
Share to Aged
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Guanine Nucleotide Exchange Factors

Share to Motor Neuron Disease

Share to Mutation

Source

Identifiers

PMID: 17698795
DOI: 10.1212/01.wnl.0000267322.48364.76

Genes

ALS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene.PMID 17698795Read ↗

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.Semantic proximity Read ↗

ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion.Semantic proximity Read ↗

Novel compound heterozygous ALS2 mutations cause juvenile amyotrophic lateral sclerosis in Japan.Semantic proximity Read ↗

UBQLN2 mutations are not a frequent cause of amyotrophic lateral sclerosis in Ireland.Semantic proximity Read ↗

Mutations in VAPB are not associated with sporadic ALS.Semantic proximity Read ↗

Deficiency in the ALS2 gene does not affect the motor neuron degeneration in SOD1(G93A) transgenic mice.Semantic proximity Read ↗

Misfolded SOD1 is not a primary component of sporadic ALSSemantic proximity Read ↗

No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population.Semantic proximity Read ↗

The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings.Semantic proximity Read ↗

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis.Semantic proximity Read ↗

UBQLN2 in familial amyotrophic lateral sclerosis in The Netherlands.Semantic proximity Read ↗

Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis.Semantic proximity Read ↗

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