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DSIP carries a tryptophan residue at its N-terminus that gives a characteristic UV signature used in laboratory identification, and in the research literature it is studied in connection with sleep regulation and circadian rhythm

(2025) 4:e70024

Wilson disease Wilson disease Wilson disease (hepatolenticular degeneration) is an autosomal recessive disorder caused by various mutations in the ATP7B gene, which regulates copper transport within hepatocytes

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