Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies
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概要
- 論文の詳細を見る
- 2012-01-01
著者
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Mathieson Iain
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Murphy Valerie
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Deng Alexander
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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PAGNAMENTA Alistair
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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LISE Stefano
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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HARRISON Victoria
Department of Clinical Genetics, Oxford Radcliffe NHS Trust
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STEWART Helen
Department of Clinical Genetics, Oxford Radcliffe NHS Trust
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JAYAWANT Sandeep
Department of Neurology, John Radcliffe Hospital
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QUAGHEBEUR Gerardine
Department of Neuroradiology, John Radcliffe Hospital
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AKHA Elham
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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RIMMER Andy
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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KNIGHT Samantha
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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KINI Usha
Department of Clinical Genetics, Oxford Radcliffe NHS Trust
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TAYLOR Jenny
NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics
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KEAYS David
Department of Neurogenetics, Research Institute of Molecular Pathology
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Keays David
Department Of Neurogenetics Research Institute Of Molecular Pathology
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Jayawant Sandeep
Department Of Neurology John Radcliffe Hospital
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Stewart Helen
Department Of Clinical Genetics Oxford Radcliffe Nhs Trust
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Taylor Jenny
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Knight Samantha
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Rimmer Andy
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Kini Usha
Department Of Clinical Genetics Oxford Radcliffe Nhs Trust
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Harrison Victoria
Department Of Clinical Genetics Oxford Radcliffe Nhs Trust
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Lise Stefano
Nihr Biomedical Research Centre Wellcome Trust Centre For Human Genetics
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Quaghebeur Gerardine
Department Of Neuroradiology John Radcliffe Hospital