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

Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.

Annals of neurology - 1 Jul 1995

Matilla T, McCall A, Subramony S H, Zoghbi H Y

Abstract excerpt

The autosomal dominant spinocerebellar ataxias are clinically and genetically a heterogeneous group of neurodegenerative disorders. Genetic studies have classified some of these disorders based on the mapping of their respective genes. The gene for Machado-Joseph disease, one type of spinocerebellar ataxia, has been mapped to the long arm of chromosome 14q24.3-ter. The gene for another spinocerebellar ataxia,...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Age of Onset
Share to Alleles

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

Share to Base Sequence

Share to Molecular Sequence Data

Share to Polymerase Chain Reaction

Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 7611728
DOI: 10.1002/ana.410380113

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.PMID 7611728Read ↗

[Recent advances in molecular genetics of spinocerebellar ataxia type 3/Machado-Joseph disease].Semantic proximity Read ↗

Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.Semantic proximity Read ↗

Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD).Semantic proximity Read ↗

Machado-Joseph Disease: from first descriptions to new perspectives.Semantic proximity Read ↗

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.Semantic proximity Read ↗

Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.Semantic proximity Read ↗

Machado Joseph disease: clinical and genetic aspects, and current treatmentSemantic proximity Read ↗

A clinical and pathologic study of a large Japanese family with Machado‐ Joseph disease tightly linked to the DNA markers on chromosome 14qSemantic proximity Read ↗

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.Semantic proximity Read ↗

Machado-Joseph disease: an autosomal dominant motor system degeneration.Semantic proximity Read ↗

Protocol for the Characterization of the Cytosine-Adenine-Guanine Tract and Flanking Polymorphisms in Machado-Joseph Disease: Impact on Diagnosis and Development of Gene-Based Therapies.Semantic proximity Read ↗

Machado‐joseph disease: Clinical, molecular, and metabolic characterization in chinese kindredsSemantic proximity Read ↗

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