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Journal Article
Journal Article
Journal of inherited metabolic disease, ISSN 0141-8955, 2018, Volume 41, Issue 2, pp. 249 - 255
Human Genetics | Biochemistry, general | Pediatrics | Medicine & Public Health | Metabolic Diseases | Zellweger spectrum disorders | Internal Medicine | Peroxisome biogenesis disorders | Coagulopathy | Vitamin K | Endocrinology & Metabolism | Genetics & Heredity | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Prospective Studies | Protein Precursors - blood | Vitamin K Deficiency - diagnosis | Humans | Netherlands - epidemiology | Vitamin K Deficiency - blood | Male | Incidence | Zellweger Syndrome - drug therapy | Young Adult | Vitamin K Deficiency - drug therapy | Female | Retrospective Studies | Vitamin K - administration & dosage | Child | Severity of Illness Index | Blood Coagulation Disorders - epidemiology | Hemorrhage - epidemiology | Vitamin K Deficiency - epidemiology | Administration, Oral | Treatment Outcome | Hemorrhage - blood | Biomarkers - blood | Zellweger Syndrome - diagnosis | Proof of Concept Study | Hemorrhage - diagnosis | Blood Coagulation Disorders - drug therapy | Administration, Intravenous | Hemorrhage - drug therapy | Pilot Projects | Blood Coagulation - drug effects | Zellweger Syndrome - blood | Adolescent | Blood Coagulation Disorders - blood | Prothrombin | Blood Coagulation Disorders - diagnosis | Dietary Supplements | Zellweger Syndrome - epidemiology | Proteins | Medical research | Medical examination | Medicine, Experimental | Medical records | Thrombin | Blood | Vitamins | Nutrient deficiency | Liver diseases | Dietary supplements |