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KD also contributed to increased sphingomyelin levels and enhanced hydroxylation of sphingomyelins and acylcarnitines, which determine changes in cell membrane composition

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Introduction Wilsons disease (WD) is a genetic disorder inherited in an autosomal recessive manner, resulting from mutations in the ATP7B gene located on chromosome 13 (13q14.3)

Estimating sensitivity of the Kato-Katz technique for the diagnosis of Schistosoma mansoni and hookworm in relation to infection intensity