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Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1

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第一作者: Nurulamin Abu Bakar
作者单位: Department of Neurology, Translational Metabolic Laboratory, Donders Institute for Brain, Cognition [1] Department of Clinical Pathology,The Sarah Network of Rehabilitation Hospitals [2] Translational Metabolic Laboratory, Department Laboratory Medicine,Radboud University Medical Center [3] Genetics Department,Kuala Lumpur Hospital, Kuala Lumpur, Ministry of Health Malaysia [4] Genetic Unit,Sarah Network of Hospitals [5] Department of Laboratory Medicine,UMC Groningen [6] Pediatric Neurology,Children's Health Ireland (CHI) [7] Metabolic Department, Great Ormond Street Hospital NHS Foundation Trust Institute of Child Health [8] Department of Enzymology and Cellular Function,Institute of Child Health [9] Genetics and Rare Diseases Research Division,Bambino Gesù Children's Research Hospital [10] Department of Internal Medicine,Radboud University Medical Center [11] Department of Pediatrics,Radboud University Medical Center [12] Department of Pediatrics, Translational Metabolic Laboratory,Radboud University Medical Center [13] Center for Child and Adolescent Medicine,Kinderheilkunde I, University of Heidelberg [14]
发布时间 2022-09-16
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