학술논문

Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting
Document Type
Article
Source
In: Human Molecular Genetics. (Human Molecular Genetics, 1 August 2010, 19(15):2987-2997)
Subject
Language
English
ISSN
09646906
14602083