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

Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34

1 Mar 1998

Abstract excerpt

We performed genetic mapping studies of an 11-generation pedigree with an autosomal dominant, juvenile-onset motor-systems disease. The disorder is characterized by slow progression, distal limb amyotrophy, and pyramidal tract signs associated with severe loss of motor neurons in the brain stem and spinal cord. The gene for this disorder, classified as a form of juvenile amyotrophic lateral sclerosis (ALS), is...

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

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9497266
DOI: 10.1086/301769

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34PMID 9497266Read ↗

Three Families With Amyotrophic Lateral Sclerosis and Frontotemporal Dementia With Evidence of Linkage to Chromosome 9pSemantic proximity Read ↗

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.Semantic proximity Read ↗

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.Semantic proximity Read ↗

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.Semantic proximity Read ↗

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.Semantic proximity Read ↗

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.Semantic proximity Read ↗

A high-resolution linkage map of human 9q34.1.Semantic proximity Read ↗

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.Semantic proximity Read ↗

A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36.Semantic proximity Read ↗

Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22Semantic proximity Read ↗

Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.Semantic proximity Read ↗

A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qterSemantic proximity Read ↗

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