Origins and evolution of huntington disease chromosomes
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neuropsychology and Physiological Psychology,Pathology and Forensic Medicine
Reference51 articles.
1. Geographical distribution of haplotypes in Swedish families with Huntington disease;Almqvist;Hum Genet,1994
2. Ancestral differences in the distribution of the Δ2642 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,1994
3. Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded repeat;Ambrose;Somat Cell Mol Genet,1994
4. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew;Nature Genet,1993
5. DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease;Andrew;Clin Genet,1993
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1. Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease;Human Molecular Genetics;2022-09-20
2. HTT haplogroups in Finnish patients with Huntington disease;Neurology Genetics;2019-04-22
3. The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2018-02-20
4. Epidemiology of Huntington disease;Huntington Disease;2017
5. Clinical and genetic characteristics in patients with Huntington’s disease from China;Neurological Research;2016-07-29
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