Fabry disease (FD) is an X-linked progressive multisystem disease due to mutations in the gene encoding the lysosomal enzyme α-galactosidase A (α-GalA). The deficiency in α-GalA activity leads to an intra-lysosomal accumulation of neutral glycosphingolipids, mainly globotriaosylceramide (Gb3), in various organs and systems. Enzyme replacement therapy is available and alternative therapeutic approaches are being explored. No diagnostic test, other than sequencing of the α-galactosidase A gene, is available, no biomarker has been proven useful to screen for and predict the disease, and underlying mechanisms are still elusive. The aim of this study is to identify FD specific biomarkers and to better understand the pathophysiological changes th...
AbstractFabry Disease (FD) is an X-linked multisystemic lysosomal disorder caused by mutations of α-...
Fabry disease (FD) is a rare X-linked recessive glycosphingolipid-storage disorder caused by deficie...
<div><p>Fabry disease (FD) is an X-linked hereditary defect of glycosphingolipid storage caused by m...
Fabry disease (FD) is an X-linked progressive multisystem disease due to mutations in the gene encod...
Fabry disease (FD) is an X-linked lysosomal rare disease due to a deficiency of α-galactosidase A ac...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the lysosomal...
International audienceBackground: Fabry disease (FD) is an X-linked progressive lysosomal disease (L...
: Fabry disease is a rare X-linked disease characterized by deficient expression and activity of alp...
Background: Fabry disease (FD) is an X-linked lysosomal disease due to a deficiency in the activity ...
Fabry disease (FD) is an X-linked lysosomal disease due to a deficiency in the activity of the lysos...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
Fabry disease (FD) is a lysosomal storage disorder, depending on defects in alphagalactosidase A (GA...
Fabry disease (FD) is a lysosomal storage disorder caused by deficient alpha-galactosidase A activit...
Fabry disease (FD) is a rare X-linked recessive genetic disorder caused by a deficient activity of t...
Fabry disease is a hereditary metabolic disorder caused by insufficient activity of the enzyme α-gal...
AbstractFabry Disease (FD) is an X-linked multisystemic lysosomal disorder caused by mutations of α-...
Fabry disease (FD) is a rare X-linked recessive glycosphingolipid-storage disorder caused by deficie...
<div><p>Fabry disease (FD) is an X-linked hereditary defect of glycosphingolipid storage caused by m...
Fabry disease (FD) is an X-linked progressive multisystem disease due to mutations in the gene encod...
Fabry disease (FD) is an X-linked lysosomal rare disease due to a deficiency of α-galactosidase A ac...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by a deficiency of the lysosomal...
International audienceBackground: Fabry disease (FD) is an X-linked progressive lysosomal disease (L...
: Fabry disease is a rare X-linked disease characterized by deficient expression and activity of alp...
Background: Fabry disease (FD) is an X-linked lysosomal disease due to a deficiency in the activity ...
Fabry disease (FD) is an X-linked lysosomal disease due to a deficiency in the activity of the lysos...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
Fabry disease (FD) is a lysosomal storage disorder, depending on defects in alphagalactosidase A (GA...
Fabry disease (FD) is a lysosomal storage disorder caused by deficient alpha-galactosidase A activit...
Fabry disease (FD) is a rare X-linked recessive genetic disorder caused by a deficient activity of t...
Fabry disease is a hereditary metabolic disorder caused by insufficient activity of the enzyme α-gal...
AbstractFabry Disease (FD) is an X-linked multisystemic lysosomal disorder caused by mutations of α-...
Fabry disease (FD) is a rare X-linked recessive glycosphingolipid-storage disorder caused by deficie...
<div><p>Fabry disease (FD) is an X-linked hereditary defect of glycosphingolipid storage caused by m...