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[Lysosomal protein 2 (LIMP2), the product of the scavenger receptor class B member 2 (SCARB2) gene, is a ubiquitously expressed transmembrane protein that is the mannose-6-phosphate-independent receptor for glucocerebrosidase (?-GCase); a deficiency in this protein causes Gaucher disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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