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This disorder is caused by an inherited deficiency of glutaryl-CoA dehydrogenase, which is involved in the catabolic pathways of L-lysine, L-hydroxylysine and L-tryptophan (97)
Zou Y-X, Ruan M-H, Luan J, Feng X, Chen S, Chu Z-Y
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Advanced Retention Systems (Gels and Nanocrystals) To transition from systemic to topical therapy, formulations must overcome rapid tear fluid washout
