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doi: 10.1113/jphysiol.2003.049478

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10.1016/j.metop.2022.100179 85

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HouYTangGWangQZhouMXuRChenXet al

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Hyperlysinemia is an autosomal recessive disorder characterized by increased lysine levels in the blood caused by a defect of the bifunctional AASA synthase

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During the COVID-19 pandemic, when a flexible approach and speedy access were needed, these pathways have provided unprecedented benefits to the sponsors who were able to bring their COVID-19 indicated medicines into Australia and have them approved and reimbursed in a timely manner and to the Australian consumer

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Each leads in a different research context

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