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Unraveling progression subtypes in people with Huntington’s disease

Unraveling progression subtypes in people with Huntington’s disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11148000

Unraveling progression subtypes in people with Huntington’s disease

About this item

Full title

Unraveling progression subtypes in people with Huntington’s disease

Publisher

Cham: Springer International Publishing

Journal title

The EPMA journal, 2024-06, Vol.15 (2), p.275-287

Language

English

Formats

Publication information

Publisher

Cham: Springer International Publishing

More information

Scope and Contents

Contents

Background
Huntington’s disease (HD) is a progressive neurodegenerative disease caused by a CAG trinucleotide expansion in the huntingtin gene. The length of the CAG repeat is inversely correlated with disease onset. HD is characterized by hyperkinetic movement disorder, psychiatric symptoms, and cognitive deficits, which greatly impact patient’...

Alternative Titles

Full title

Unraveling progression subtypes in people with Huntington’s disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11148000

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11148000

Other Identifiers

ISSN

1878-5077,1878-5085

E-ISSN

1878-5085

DOI

10.1007/s13167-024-00368-2

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