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

Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genes.

Neurogenetics - 1 Sept 2004

Kok Cindy, Kennerson Marina L, Myers Simon J, Nicholson Garth A

Abstract excerpt

Dominantly inherited sensory neuropathy (HSNI) is a degenerative disorder of sensory neurons characterized predominantly by sensory loss with mild motor impairment. Recently our group identified a locus on chromosome 3p for a new form of HSNI associated with cough and gastroesophageal reflux (GER). Haplotype analysis in a second family refined the interval to a 3.4-cM region that includes the candidate genes...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 3
Share to Computational Biology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gastroesophageal Reflux

Share to Genome, Human

Share to Hereditary Sensory and Motor Neuropathy

Share to Neurons

Share to Physical Chromosome Mapping

Source

Identifiers

PMID: 15241656
DOI: 10.1007/s10048-004-0185-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genes.PMID 15241656Read ↗

Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes.Semantic proximity Read ↗

Intronic variant in IQGAP3 associated with hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry cough.Semantic proximity Read ↗

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.Semantic proximity Read ↗

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.Semantic proximity Read ↗

Refined mapping of the HMSNR critical gene region--construction of a high-density integrated genetic and physical map.Semantic proximity Read ↗

TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disabilitySemantic proximity Read ↗

A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2.Semantic proximity Read ↗

The Charcot-Marie-Tooth Neuropathy (CMTX3) Complex Structural Variation Causes Differential SOX3 Spatiotemporal ExpressionSemantic proximity Read ↗

Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia.Semantic proximity Read ↗

Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genes.Semantic proximity Read ↗

A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain.Semantic proximity Read ↗

Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.Semantic proximity Read ↗

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