Agalsidase alfa in pediatric patients with Fabry disease: a...

Orphanet Journal of Rare Diseases 2014 / 12 Vol. 9; Iss. 1

Agalsidase alfa in pediatric patients with Fabry disease: a 6.5-year open-label follow-up study

Schiffmann, Raphael, Pastores, Gregory M, Lien, Yeong-Hau H, Castaneda, Victoria, Chang, Peter, Martin, Rick, Wijatyk, Anna
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Volume:
9
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-014-0169-6
Date:
December, 2014
File:
PDF, 800 KB
english, 2014
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