Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiency

Jean-Claude Michalski1, André Klein2
1Laboratoire de Chimie Biologique, UMR 8576 CNRS (UMR 111 CNRS), Université des Sciences et Technologies de Lille, 59655 Villeneuve d’Ascq Cedex, France
2Unité 377 INSERM, C.H.U., Place de Verdun, 59045 Lille Cedex, France

Tài liệu tham khảo

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