Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Huntington's disease pathogenesis: two sequential components

Hong, Eun Pyo, MacDonald, Marcy E., Wheeler, Vanessa C., Jones, Lesley, Holmans, Peter, Orth, Michael, Monckton, Darren G., Long, Jeffrey D., Kwak, Seung, Gusella, James F., Lee, Jong-Min, Jones, Lesley, Pearson, Christopher E. and Wheeler, Vanessa 2021. Huntington's disease pathogenesis: two sequential components. Journal of Huntington's Disease 10 (1) , pp. 35-51. 10.3233/JHD-200427

[thumbnail of jhd_2021_10-1_jhd-10-1-jhd200427_jhd-10-jhd200427.pdf] PDF - Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (2MB)

Abstract

Historically, Huntington’s disease (HD; OMIM #143100) has played an important role in the enormous advances in human genetics seen over the past four decades. This familial neurodegenerative disorder involves variable onset followed by consistent worsening of characteristic abnormal movements along with cognitive decline and psychiatric disturbances. HD was the first autosomal disease for which the genetic defect was assigned to a position on the human chromosomes using only genetic linkage analysis with common DNA polymorphisms. This discovery set off a multitude of similar studies in other diseases, while the HD gene, later renamed HTT, and its vicinity in chromosome 4p16.3 then acted as a proving ground for development of technologies to clone and sequence genes based upon their genomic location, with the growing momentum of such advances fueling the Human Genome Project. The identification of the HD gene has not yet led to an effective treatment, but continued human genetic analysis of genotype-phenotype relationships in large HD subject populations, first at the HTT locus and subsequently genome-wide, has provided insights into pathogenesis that divide the course of the disease into two sequential, mechanistically distinct components.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Additional Information: This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC 4.0).
Publisher: IOS Press
ISSN: 1879-6397
Funders: MRC, CHDI
Date of First Compliant Deposit: 9 December 2021
Date of Acceptance: 31 July 2020
Last Modified: 09 Dec 2021 13:45
URI: https://orca.cardiff.ac.uk/id/eprint/145991

Citation Data

Cited 16 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics