[HTML][HTML] Fabry disease
DP Germain - Orphanet journal of rare diseases, 2010 - Springer
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
Fabry disease.
DP Germain - Orphanet Journal of Rare Diseases, 2010 - europepmc.org
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
Fabry disease
DP Germain - Orphanet Journal of Rare Diseases, 2010 - search.proquest.com
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
Fabry disease
DP Germain - Orphanet journal of rare diseases, 2010 - pubmed.ncbi.nlm.nih.gov
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
[PDF][PDF] Fabry disease
DP Germain - 2010 - cyberleninka.org
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
[HTML][HTML] Fabry disease
DP Germain - Orphanet Journal of Rare Diseases, 2010 - ojrd.biomedcentral.com
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal α-galactosidase A activity. FD is pan-ethnic …
[PDF][PDF] Fabry disease
DP Germain - 2010 - scienceopen.com
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
[PDF][PDF] Fabry disease
DP Germain - 2010 - Citeseer
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
metabolism due to deficient or absent lysosomal a-galactosidase A activity. FD is pan-ethnic …
Fabry disease
DP Germain - Orphanet Journal of Rare Diseases, 2010 - go.gale.com
Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid
metabolism due to deficient or absent lysosomal [alpha]-galactosidase A activity. FD is pan …
metabolism due to deficient or absent lysosomal [alpha]-galactosidase A activity. FD is pan …