Risk factors for the onset and progression of Huntington disease-Reference-Cited by-同舟云学术

Risk factors for the onset and progression of Huntington disease

Published:2017-07 Issue: Volume:61 Page:79-99
ISSN:0161-813X
Container-title:NeuroToxicology
language:en
Short-container-title:NeuroToxicology

Author:

Chao Ting-Kuang,Hu Jing,Pringsheim Tamara

Funder

Public Health Agency of Canada in association with Neurological Health Charities Canada through a contribution agreement administered through the University of Ottawa

Publisher

Elsevier BV

Subject

Toxicology,General Neuroscience

Reference172 articles.

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3. Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease;Almqvist;Hum. Mol. Genet.,1995

4. Clinical and genetic characteristics of Mexican Huntington’s disease patients;Alonso;Mov. Disord.,2009

5. The relationship between CAG repeat length and, age of onset differs for Huntington’s disease patients with juvenile onset or adult onset;Andresen;Ann. Hum. Genet.,2007

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