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Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features

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作者单位: Institute of Pharmacology and Toxicology, University of Zürich-VetsuisseZürich, Switzerland [1] Bioinformatics Division, Walter and Eliza Hall InstituteParkville, VIC, Australia, Department of [2] Bioinformatics Division, Walter and Eliza Hall InstituteParkville, VIC, Australia [3] Unidad de Investigación, Hospital Universitario de Canarias, Instituto de Tecnologías BiomédicasLa [4] Victorian Clinical Genetics Services, Murdoch Childrens Research InstituteParkville, VIC, Australia [5] Institute of Human Genetics, University of UlmUlm, Germany, Institute of Human Genetics, University [6] Department of Pathology, University of WashingtonSeattle, WA, United States [7] Cologne Center for Genomics, University of CologneCologne, Germany [8] Institute of Genetics, University of CologneCologne, Germany [9] Cancer Research UK and Medical Research Council Oxford Institute for Radiation Oncology, Department [10] Cologne Center for Genomics, University of CologneCologne, Germany, Center for Molecular Medicine [11] Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research InstituteParkville, VIC [12] Buchmann Institute for Molecular Life Sciences, Goethe UniversityFrankfurt (Main), Germany [13] Department of Clinical Genetics, Amsterdam Medical CentreAmsterdam, Netherlands [14] Institute of Human Genetics, University of UlmUlm, Germany [15] Department of Immunology and Medical Genetics, University of Split, School of MedicineSplit, Croatia [16] Department of Biochemistry and Molecular Biology, University of UlmUlm, Germany [17] Leibniz Institute for Age Research, Fritz Lippmann InstituteJena, Germany [18]
发布时间 2014-12-20
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Nature Genetics

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