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Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease
Rafael Bretón Martínez, J., Martínez, Andrés CánovasLanguage:
english
Journal:
Journal of the Neurological Sciences
DOI:
10.1016/j.jns.2015.08.007
Date:
August, 2015
File:
PDF, 191 KB
english, 2015