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Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.
Li, Mingkun; Rothwell, Rebecca; Vermaat, Martijn; Wachsmuth, Manja; Schröder, Roland; Laros, Jeroen F J; van Oven, Mannis; de Bakker, Paul I W; Bovenberg, Jasper A; van Duijn, Cornelia M; van Ommen, Gert-Jan B; Slagboom, P Eline; Swertz, Morris A; Wijmenga, Cisca; Kayser, Manfred; Boomsma, Dorret I; Zöllner, Sebastian; de Knijff, Peter; Stoneking, Mark.
Afiliação
  • Li M; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany; Fondation Mérieux, 69002 Lyon, France;
  • Rothwell R; Department of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA;
  • Vermaat M; Leiden Genome Technology Center, Department of Human Genetics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands;
  • Wachsmuth M; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany;
  • Schröder R; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany;
  • Laros JF; Leiden Genome Technology Center, Department of Human Genetics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands;
  • van Oven M; Department of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam 3000 CA, The Netherlands;
  • de Bakker PI; Department of Medical Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht 3584 CG, The Netherlands; Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht 3584 CG, The Netherlands;
  • Bovenberg JA; Department of Biological Psychology, VU University Amsterdam, Amsterdam 1081 BT, The Netherlands;
  • van Duijn CM; Legal Pathways Institute for Health and Bio Law, Aerdenhout 2111, The Netherlands;
  • van Ommen GJ; Department of Epidemiology, Erasmus MC University Medical Center Rotterdam, Rotterdam 3000 CA, The Netherlands;
  • Slagboom PE; Department of Human Genetics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands;
  • Swertz MA; Section of Molecular Epidemiology, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen 9700 RB, The Netherlands;
  • Wijmenga C; Section of Molecular Epidemiology, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen 9700 RB, The Netherlands;
  • Kayser M; Department of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam 3000 CA, The Netherlands;
  • Boomsma DI; Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen 9700 RB, The Netherlands;
  • Zöllner S; Department of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA; Department of Psychiatry, University of Michigan, Ann Arbor, Michigan 48109, USA.
  • de Knijff P; Department of Human Genetics, Leiden University Medical Center, Leiden 2300 RC, The Netherlands;
  • Stoneking M; Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany;
Genome Res ; 26(4): 417-26, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26916109
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Família / Heterogeneidade Genética / Padrões de Herança / População Branca Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Genome Res Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Família / Heterogeneidade Genética / Padrões de Herança / População Branca Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Genome Res Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2016 Tipo de documento: Article