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Article

Huntington's disease.

Prenatal diagnosis - 1 Dec 1996

Craufurd D

Abstract excerpt

Huntington's disease (HD) is a late-onset degenerative disorder of the central nervous system, caused by a dominantly inherited mutation in a gene on chromosome 4p. The identification of the trinucleotide repeat mutation responsible for this disorder has been an important step towards understanding the molecular pathology of HD, but in the meantime has also made it possible to offer predictive testing and...

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Identifiers

PMID: 9061754
DOI: 10.1002/(SICI)1097-0223(199612)16:13<1237::AID-PD98>3.0.CO;2-T

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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.

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