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Maple Syrup Urine Disease | Pathogenesis, Signs & Symptoms, Subtypes, Diagnosis and Treatment - YouTube
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Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations | SpringerLink
CENTOGENE - Did you know? #DUK Maple syrup urine disease #Didyouknow Maple syrup urine disease is an inherited metabolic disorder, in which the body is unable to process amino acids from protein
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PPT - Maple Syrup Urine Disease (MSUD) By Jenny Morrison (836445) PowerPoint Presentation - ID:334267
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Genetic analysis by targeted next-generation sequencing and novel variation identification of maple syrup urine disease in Chinese Han population | Scientific Reports
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Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes - ScienceDirect
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Pathophysiology of maple syrup urine disease: Focus on the neurotoxic role of the accumulated branched-chain amino acids and branched-chain α-keto acids - ScienceDirect
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