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

Update on Genetic Chorea.

Current neurology and neuroscience reports - 4 Jul 2026

Ostrozovicova Miriam, Skorvanek Matej

Abstract excerpt

PURPOSE OF REVIEW: Chorea is a symptom of numerous pathophysiologically and clinically heterogeneous genetic conditions. A number of developments have been made in this field over the last years linked to improved genomic testing, large cohort collaborations and improved understanding of the molecular mechanisms. This review aims to provide an update on the new genetic conditions and phenotypes linked to chorea...

Read the complete abstract on PubMed

Topics

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

Share to Chorea
Share to HTT gene
Share to Mutation

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

Source

Open in PubMed Open full text

Identifiers

PMID: 42400823
DOI: 10.1007/s11910-026-01502-5
PMCID: PMC13332979

Genes

ACBD6
FTH1
HTT
NAA60
TOR1AIP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 15 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

Update on Genetic Chorea.PMID 42400823Read ↗

Recent advances in genetics of chorea.Semantic proximity Read ↗

Non-HD-Chorea: An Expanding UniverseSemantic proximity Read ↗

Huntington's disease and Huntington's disease-like syndromes: an overview.Semantic proximity Read ↗

Chorea: An Update on Genetics.Semantic proximity Read ↗

Chorea.Semantic proximity Read ↗

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

Beyond CAG Repeats: The Multifaceted Role of Genetics in Huntington DiseaseSemantic proximity Read ↗

The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.Semantic proximity Read ↗

Huntington's disease: new aspects on phenotype and genotype.Semantic proximity Read ↗

Huntington's disease: a clinical reviewSemantic proximity Read ↗

Microsatellite expansions hidden within the human dark genome are translated in novel and toxic proteins causing muscle and neurodegenerative diseasesSemantic proximity Read ↗

[Huntington´s disease - overview].Semantic proximity Read ↗

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