Glycogen storage in a zebrafish Pompe disease model is reduced by 3-BrPA treatment

Author:

Bragato Cinzia,Carra Silvia,Blasevich Flavia,Salerno Franco,Brix Alessia,Bassi Andrea,Beltrame Monica,Cotelli Franco,Maggi Lorenzo,Mantegazza Renato,Mora Marina

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference63 articles.

1. Pompe disease: from basic science to therapy;Kohler;Neurotherapeutics,2018

2. Acid Maltase Deficiency. New York;Engel,2004

3. How to describe the clinical spectrum in Pompe disease?;Güngör;Am. J. Med. Genet.,2013

4. Enzyme replacement therapy in the mouse model of Pompe disease;Raben;Mol. Genet. Metab.,2003

5. Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk;Van den Hout;Pediatrics,2004

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