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

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

Genome - 1 Nov 2008

Dick Katherine J, McEntagart Meriel, Alwan Wisam, Reilly Mary, Crosby Andrew H

Abstract excerpt

Distal hereditary motor neuronopathy type seven (dHMN-VII) is an autosomal dominant condition characterized by distal muscular atrophy associated with unilateral or bilateral vocal cord paralysis. We previously mapped the dHMN-VII locus to chromosome 2q14 using a genome-wide linkage scan in a single large pedigree. Here we have performed more detailed microsatellite saturation analysis and also evaluated two new...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Primers

Share to Genes, Dominant

Share to Hereditary Sensory and Motor Neuropathy

Share to Microsatellite Repeats

Share to Pedigree

Share to Young Adult

Source

Identifiers

PMID: 18956029
DOI: 10.1139/G08-078

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genes.PMID 18956029Read ↗

Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14Semantic proximity Read ↗

A 1.35 Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2.Semantic proximity Read ↗

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

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.Semantic proximity Read ↗

Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.Semantic proximity Read ↗

Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15Semantic proximity Read ↗

The gene for HMSN2C maps to 12q23-24Semantic proximity Read ↗

Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.Semantic proximity Read ↗

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

Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): A potential susceptibility factor for adult-onset lower motor neuron diseaseSemantic proximity Read ↗

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

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.Semantic proximity Read ↗

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