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Article

Autosomal dominant cerebellar ataxias in the Kinki area of Japan.

The Japanese journal of human genetics - 1 Dec 1996

Matsumura R, Takayanagi T, Murata K, Futamura N, Fujimoto Y

Abstract excerpt

The autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders characterized by slowly progressive cerebellar ataxia. Recently, among the ataxias, spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD) and dentatorubral-pallidoluysian atrophy have been found to be caused by expansion of a CAG trinucleotide repeat in the coding region of the disease genes. We have...

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PMID: 9088110
DOI: 10.1007/BF01876330

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

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