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Article

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

Journal of the neurological sciences - 1 Sept 1995

Haberhausen G, Damian M S, Leweke F, Müller U

Abstract excerpt

Spinocerebellar ataxia, type 3 (SCA3) and Machado-Joseph disease (MJD) are two clinically distinct representatives of the heterogeneous group of autosomal dominant cerebellar ataxias. Assignment of the disease genes to the same region of the long arm of chromosome 14 in both SCA3 and MJD suggeste...

Topics

Chromosome Mapping
Chromosomes, Human, Pair 14
Female
Genes, Dominant
Humans
Machado-Joseph Disease
Male
Middle Aged
Mutation
Pedigree
Repetitive Sequences, Nucleic Acid
Spinocerebellar Degenerations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8523034
DOI: 10.1016/0022-510x(95)90927-i

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8523034-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD).PMID 8523034Read ↗

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