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pro vyhledávání: '"G De La Morena"'
Autor:
M.A. Quintanilla, Francisco Marcos Marín, Diana Hernández-Romero, Luis Caballero, G. de la Morena, Vicente Climent
Publikováno v:
Current Medicinal Chemistry. 17:1679-1689
Fabry disease (FD) is an X-linked glycosphingolipid storage disorder caused by deficient activity of the lysosomal enzyme alpha-galactosidase A. This leads to a progressive accumulation of globotriaosylceramide (Gb3) in the lysosomes of different cel