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[Given the similarity of the storage cells in NPD and Gaucher disease, we studied Gaucher plasma markers (chitotriosidase and CCL18) in two siblings homozygous for the R228C mutation in acid sphingomyelinase (ASM) and a type B course of NPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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