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human glutathione synthetase inhibitor Synthase - an overview Wholesale Inventory wells fargo dsip managed Size:90 COUNT
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A Mendelian Disease Caused by Mutations in ATP7B WD is a well-established monogenic condition caused by deleterious variants in ATP7B inherited in an autosomal recessive manner [66,67]
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Recent studies additionally suggested a role of cerebellar astrocytes
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