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Publikováno v:
Postgraduate Medical Journal
Fabry disease is a rare inborn error of the enzyme α-galactosidase (α-Gal) and results in lysosomal substrate accumulation in tissues with a wide range of clinical presentations. The disease has attracted a lot of interest over the last years, in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75e99f47b39a07189e6aed3f287d7f07
https://doi.org/10.1136/postgradmedj-2018-136056
https://doi.org/10.1136/postgradmedj-2018-136056
