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Article

Genotype-phenotype correlation in CAG-repeat diseases.

Neuropathology : official journal of the Japanese Society of Neuropathology - 1 Dec 2002

Yamada Mitsunori, Tsuji Shoji, Takahashi Hitoshi

Abstract excerpt

The expansion of a CAG repeat is a common causative gene mutation in several hereditary neurodegenerative disorders, including dentatorubral-pallidoluysian atrophy (DRPLA). Although, in DRPLA, it is revealed that the variety of clinical manifestations is related to the variable expansion of the CAG repeat, there are still many problems in the correlation between the symptoms and neuropathologic findings. Recent...

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PMID: 12564773
DOI: 10.1046/j.1440-1789.2002.00457.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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