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

Multiple clinical features of Huntington’s disease correlate with mutant HTT gene CAG repeat lengths and neurodegeneration

28 Jun 2018

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 Genetic Neurodegenerative Diseases
Share to Mitochondrial Function and Pathology
Share to Neurological disorders and treatments

Source

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

Identifiers

PMID: 29956026
DOI: 10.1007/s00415-018-8940-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 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

Multiple clinical features of Huntington’s disease correlate with mutant HTT gene CAG repeat lengths and neurodegenerationPMID 29956026Read ↗

Huntington disease.Semantic proximity Read ↗

Somatic CAG repeat expansion in blood associates with biomarkers of neurodegeneration in Huntington’s disease decades before clinical motor diagnosisSemantic proximity Read ↗

The clinical and genetic features of Huntington disease.Semantic proximity Read ↗

Association of CAG Repeats With Long-term Progression in Huntington DiseaseSemantic proximity Read ↗

A systematic review of the intergenerational aspects and the diverse genetic profiles of Huntington's disease.Semantic proximity Read ↗

Challenges of the Polyglutamine Diseases: From Dysfunctional Neuronal Circuitries to Neuron-Specific CAG Repeat InstabilitySemantic proximity Read ↗

Genetics and neuropathology of Huntington's disease.Semantic proximity Read ↗

Huntington’s Disease: From Genetics to TherapeuticsSemantic proximity Read ↗

Exploring molecular mechanisms, therapeutic strategies, and clinical manifestations of Huntington’s diseaseSemantic proximity Read ↗

The neurology and natural history of patients with indeterminate CAG repeat length mutations of the Huntington disease gene.Semantic proximity Read ↗

Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study.Semantic proximity Read ↗

Huntingtonʼs diseaseSemantic proximity Read ↗

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