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

Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations.

Journal of voice : official journal of the Voice Foundation - 1 Jan 2017

Gómez-Coello Annel, Valadez-Jiménez Victor Manuel, Cisneros Bulmaro, Carrillo-Mora Paul, Parra-Cárdenas Martha, Hernández-Hernández Oscar, Magaña Jonathan J

Abstract excerpt

BACKGROUND/OBJECTIVES: Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by the expansion of a cytosine-adenine-guanine triplet located in the coding region of the ATXN7 gene, which is characterized by cerebellar ataxia, pigmentary macular degeneration, and dysarthria. Although dysarthria is a common feature in various SCA, its clinical characterization has been barely...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Ataxin-7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to DNA Mutational Analysis

Share to Genetic Predisposition to Disease

Share to Mexico

Share to Phenotype

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 26992556
DOI: 10.1016/j.jvoice.2016.01.010

Genes

ATXN7

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

Voice Alterations in Patients With Spinocerebellar Ataxia Type 7 (SCA7): Clinical-Genetic Correlations.PMID 26992556Read ↗

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.Semantic proximity Read ↗

Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.Semantic proximity Read ↗

Voice in Friedreich Ataxia.Semantic proximity Read ↗

Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.Semantic proximity Read ↗

Spinocerebellar ataxia 7 (SCA7).Semantic proximity Read ↗

SCA7 mouse cerebellar pathology reveals preferential downregulation of key Purkinje cell-identity genes and shared disease signature with SCA1 and SCA2.Semantic proximity Read ↗

Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansionSemantic proximity Read ↗

Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis.Semantic proximity Read ↗

Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype.Semantic proximity Read ↗

[Clinical feature and molecular genetics of hereditary spinocerebellar ataxia].Semantic proximity Read ↗

A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7.Semantic proximity Read ↗

Deciphering the natural history of SCA7 in children.Semantic proximity Read ↗

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