DOI:
10.1055/s-00029022
Journal of Pediatric Biochemistry
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References
Vaccaro AM, Motta M, Tatti M , et al.
Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting.
Hum Mol Genet 2010;
19 (15) 2987-2997
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