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The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.
Kay, Chris; Collins, Jennifer A; Wright, Galen E B; Baine, Fiona; Miedzybrodzka, Zosia; Aminkeng, Folefac; Semaka, Alicia J; McDonald, Cassandra; Davidson, Mark; Madore, Steven J; Gordon, Erynn S; Gerry, Norman P; Cornejo-Olivas, Mario; Squitieri, Ferdinando; Tishkoff, Sarah; Greenberg, Jacquie L; Krause, Amanda; Hayden, Michael R.
  • Kay C; Centre for Molecular Medicine Therapeutics, University of British Columbia, Vancouver, BC, Canada.
  • Collins JA; Centre for Molecular Medicine Therapeutics, University of British Columbia, Vancouver, BC, Canada.
  • Wright GEB; Centre for Molecular Medicine Therapeutics, University of British Columbia, Vancouver, BC, Canada.
  • Baine F; Division of Human Genetics, Department of Pathology, University of Cape Town, South Africa.
  • Miedzybrodzka Z; Division of Human Genetics, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
  • Aminkeng F; Medical Genetics Group, School of Medicine and Dentistry, University of Aberdeen, Aberdeen, UK.
  • Semaka AJ; Centre for Molecular Medicine Therapeutics, University of British Columbia, Vancouver, BC, Canada.
  • McDonald C; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research (A*STAR), Singapore.
  • Davidson M; Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
  • Madore SJ; Centre for Molecular Medicine Therapeutics, University of British Columbia, Vancouver, BC, Canada.
  • Gordon ES; Medical Genetics Group, School of Medicine and Dentistry, University of Aberdeen, Aberdeen, UK.
  • Gerry NP; Molecular Biology Group, Coriell Institute for Medical Research, Camden, New Jersey.
  • Cornejo-Olivas M; Molecular Biology Group, Coriell Institute for Medical Research, Camden, New Jersey.
  • Squitieri F; Molecular Biology Group, Coriell Institute for Medical Research, Camden, New Jersey.
  • Tishkoff S; Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.
  • Greenberg JL; IRCCS Casa Sollievo della Sofferenza Hospital, Huntington and Rare Diseases Unit (CSS-Mendel Rome), San Giovanni Rotondo, Italy.
  • Krause A; Department of Genetics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Hayden MR; Division of Human Genetics, Department of Pathology, University of Cape Town, South Africa.
Am J Med Genet B Neuropsychiatr Genet ; 177(3): 346-357, 2018 04.
Article en En | MEDLINE | ID: mdl-29460498
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Huntington Tipo de estudio: Prevalence_studies / Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Huntington Tipo de estudio: Prevalence_studies / Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article