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BRENDA support

Literature summary for 3.2.1.117 extracted from

  • Sun, B; Fredrickson, K; Austin, S; Tolun, AA; Thurberg, BL; Kraus, WE; Bali, D; Chen, YT; Kishnani, PS
    Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III. (2013), Mol Genet Metab, 108, 145-7.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining