Twenty-four-month α-galactosidase A replacement therapy in Fabry disease has only minimal effects on symptoms and cardiovascular parameters




Koskenvuo J., Hartiala J., Nuutila P., Kalliokoski R., Viikari J., Engblom E., Penttinen M., Knuuti J., Mononen I., Kantola I.

2008

 Journal of Inherited Metabolic Disease

Journal of Inherited Metabolic Disease

31

3

432

441

10

01418955 15732665

DOIhttps://doi.org/10.1007/s10545-008-0848-3

https://api.elsevier.com/content/abstract/scopus_id/45849123200




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