The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population

Author:

Kay Chris1,Collins Jennifer A.1,Wright Galen E.B.1,Baine Fiona23,Miedzybrodzka Zosia4,Aminkeng Folefac15,Semaka Alicia J.6,McDonald Cassandra1,Davidson Mark4,Madore Steven J.7,Gordon Erynn S.7,Gerry Norman P.7,Cornejo-Olivas Mario8,Squitieri Ferdinando9,Tishkoff Sarah10,Greenberg Jacquie L.2,Krause Amanda11,Hayden Michael R.1ORCID

Affiliation:

1. Centre for Molecular Medicine Therapeutics; University of British Columbia; Vancouver BC Canada

2. Division of Human Genetics; Department of Pathology; University of Cape Town; South Africa

3. Division of Human Genetics; School of Pathology; Faculty of Health Sciences; University of the Witwatersrand; Johannesburg South Africa

4. Medical Genetics Group; School of Medicine and Dentistry; University of Aberdeen; Aberdeen UK

5. Translational Laboratory in Genetic Medicine; Agency for Science, Technology and Research (A*STAR); Singapore

6. Department of Psychiatry; University of British Columbia; Vancouver BC Canada

7. Molecular Biology Group; Coriell Institute for Medical Research; Camden, New Jersey

8. Neurogenetics Research Center; Instituto Nacional de Ciencias Neurologicas; Lima Peru

9. IRCCS Casa Sollievo della Sofferenza Hospital; Huntington and Rare Diseases Unit (CSS-Mendel Rome); San Giovanni Rotondo Italy

10. Department of Genetics; School of Medicine; University of Pennsylvania; Philadelphia, Pennsylvania

11. Division of Human Genetics; National Health Laboratory Service and School of Pathology; Faculty of Health Sciences; University of the Witwatersrand; Johannesburg South Africa

Funder

Canadian Institutes of Health Research

Canadian Institutes of Health Research Doctoral Research Award

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference51 articles.

1. [Population genetic study of Huntington's disease-prevalence and founder's effect in the San-in area, western Japan];Adachi;Nihon Rinsho,1999

2. 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;Human Molecular Genetics,1995

3. Clinical and genetic characteristics of Mexican Huntington's disease patients;Alonso;Movement Disorders,2009

4. Origins and evolution of Huntington disease chromosomes;Andrew;Neurodegeneration,1995

5. Intermediate alleles of Huntington's disease HTT gene in different populations worldwide: A systematic review;Apolinario;Genetics and Molecular Research,2017

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