Huntington's Disease Gene Hunters: An Expanding Tale-Reference-Cited by-同舟云学术

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Huntington's Disease Gene Hunters: An Expanding Tale

Published:2021-12-16 Issue: Volume: Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Rosser Anne E.¹²³,Jones Lesley¹

Affiliation:

1. MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences Cardiff University School of Medicine Cardiff United Kingdom

2. Cardiff Brain Repair Group Cardiff University School Biosciences Cardiff United Kingdom

3. Wales Brain Research And Intracranial Neurotherapeutics (BRAIN) Unit Cardiff United Kingdom

Funder

Cure Huntington's Disease Initiative

H2020 Marie Skłodowska-Curie Actions

Health and Care Research Wales

UK Research and Innovation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13375

Reference38 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes;MacDonald ME;Cell,1993

2. A polymorphic DNA marker genetically linked to Huntington's disease;Gusella JF;Nature,1983

3. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu Y;Cell,1991

4. Androgen receptor gene mutations in X‐linked spinal and bulbar muscular atrophy;La Spada AR;Nature,1991

5. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy;Harley H;Nature,1992

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