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Aspartylglucosaminidase (AGA) is efficiently produced and endocytosed by glial cells: implication for the therapy of a lysosomal storage disorder
Authors:Harkke Salli  Laine Minna  Jalanko Anu
Affiliation:National Public Health Institute, Department of Molecular Medicine, and Center of Excellence in Disease Genetics, The Academy of Finland, Biomedicum, National Public Health Institute, PL-104, FIN-00251 Helsinki, Finland.
Abstract:
Keywords:adenovirus  promoter  aspartylglucosaminidase  aspartylglucosaminuria  endocytosis  lysosomal enzyme
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