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

Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis

2 Jul 2013

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 Amyotrophic Lateral Sclerosis Research
Share to Neurological diseases and metabolism
Share to Prion Diseases and Protein Misfolding

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23827524
DOI: 10.1016/j.neurobiolaging.2013.05.025

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

Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosisPMID 23827524Read ↗

Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implicationsSemantic proximity Read ↗

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortSemantic proximity Read ↗

TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutationsSemantic proximity Read ↗

Genetics of amyotrophic lateral sclerosis: A reviewSemantic proximity Read ↗

hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes.Semantic proximity Read ↗

Genetics of amyotrophic lateral sclerosisSemantic proximity Read ↗

Genotype-phenotype association and functional analysis of hnRNPA1 mutations in amyotrophic lateral sclerosis.Semantic proximity Read ↗

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosisSemantic proximity Read ↗

Emerging roles of hnRNP A2B1 in cancer and inflammationSemantic proximity Read ↗

Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosisSemantic proximity Read ↗

Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.Semantic proximity Read ↗

Genetic testing in amyotrophic lateral sclerosis.Semantic proximity Read ↗

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