首页> European journal of human genetics: EJHG> Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.

导出原文传递

翻译打印收藏纠错

第一作者： Elke de Boer

作者： Elke de Boer ^[1] ; Charlotte W Ockeloen ^[2] ; Leslie Matalonga ^[3] ; Rita Horvath ^[4] ; Solve-RD SNV-indel working group ^[5] ; Richard J Rodenburg ^[6] ; Marieke J H Coenen ^[7] ; Mirian Janssen ^[8] ; Dylan Henssen ^[9] ; Christian Gilissen ^[10] ; Wouter Steyaert ^[11] ; Ida Paramonov ; Solve-RD-DITF-ITHACA ; Aurélien Trimouille ; Tjitske Kleefstra ; Alain Verloes ; Lisenka E L M Vissers

作者单位： CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology ^[1] Department of Clinical Neurosciences, University of Cambridge, John Van Geest Cambridge Centre for ^[2] Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud ^[3] Department of Laboratory Medicine, Translational Metabolic Laboratory, Radboud University Medical ^[4] Department of Human Genetics, Radboud University Medical Center ^[5] Service de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux ^[6] Department of Internal Medicine, Radboud University Medical Center ^[7] Département de Génétique ^[8] Department of Human Genetics, Radboud Institute for Health Sciences, Radboud University Medical ^[9] Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University ^[10] Department of Medical Imaging, Radboud University Medical Center ^[11]

发布时间 2021-12-02

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交