Sign Up to like & get
recommendations!
1
Published in 2018 at "Journal of the American Society of Nephrology : JASN"
DOI: 10.1681/asn.2018030329
Abstract: Fabry disease (FD) is an X-linked lysosomal storage disorder (LSD) caused by mutations of the α-galactosidase A gene. The lysosomal enzyme α -galactosidase A (GLA) mediates the hydrolysis of the terminal α -galactosyl moiety from…
read more here.
Keywords:
replacement therapy;
therapy antidrug;
effects enzyme;
enzyme replacement ... See more keywords