Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting.
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L. Masuelli | M. Motta | A. Tylki-Szymańska | M. Vanier | R. Salvioli | A. M. Vaccaro | M. Tatti | S. Scarpa | M. Bhat