Enzyme replacement therapy in Fabry disease: Comparison of agalsidase alfa and agalsidase beta

Atul Mehta; Michael Beck; Christoph Kampmann; Andrea Frustaci; Dominique P. Germain; Gregory M. Pastores; Gere Sunder-Plassmann

doi:10.1016/j.ymgme.2008.07.002

Enzyme replacement therapy in Fabry disease: Comparison of agalsidase alfa and agalsidase beta

Atul Mehta, Michael Beck, Christoph Kampmann, Andrea Frustaci, Dominique P. Germain, Gregory M. Pastores, Gere Sunder-Plassmann

Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	114-115
Number of pages	2
Journal	Molecular Genetics and Metabolism
Volume	95
Issue number	1-2
DOIs	https://doi.org/10.1016/j.ymgme.2008.07.002
Publication status	Published - Sep 2008

ASJC Scopus subject areas

Biochemistry
Genetics
Endocrinology, Diabetes and Metabolism

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10.1016/j.ymgme.2008.07.002

Cite this

Mehta, A., Beck, M., Kampmann, C., Frustaci, A., Germain, D. P., Pastores, G. M., & Sunder-Plassmann, G. (2008). Enzyme replacement therapy in Fabry disease: Comparison of agalsidase alfa and agalsidase beta. Molecular Genetics and Metabolism, 95(1-2), 114-115. https://doi.org/10.1016/j.ymgme.2008.07.002

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