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human glutathione synthetase inhibitor deficiency Size:90 COUNT Wholesale Inventory wells fargo dsip managed
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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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Size:90 COUNT
Shubha MC, Reddy RR, Srinivasan K
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