Lysosomal leukocyte β-d-glucuronidase during enzyme replacement therapy in Fabry disease
G. Goi, Luca Massaccesi, Alessandro P. Burlina, C.J. Baquero Herrera, Adriana Lombardo, Guido Tettamanti, Alberto Burlina
Abstract
Open-access reader
G. Goi, Luca Massaccesi, Alessandro P. Burlina, C.J. Baquero Herrera, Adriana Lombardo, Guido Tettamanti, Alberto Burlina
Abstract
Open-access reader
An abstract is not available in the OpenAlex record for this paper.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Key concepts: Enzyme replacement therapy, Fabry disease, Alpha-galactosidase, Glucuronidase, Lysosomal storage disease, Enzyme, Beta-glucuronidase, Substrate reduction therapy