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BRENDA support

Literature summary for 3.2.1.117 extracted from

  • Matsuoka, T; Miwa, Y; Tajika, M; Sawada, M; Fujimaki, K; Soga, T; Tomita, H; Uemura, S; Nishino, I; Fukuda, T; Sugie, H; Kosuga, M; Okuyama, T; Umeda, Y
    Divergent clinical outcomes of alpha-glucosidase enzyme replacement therapy in two siblings with infantile-onset Pompe disease treated in the symptomatic or pre-symptomatic state. (2016), Mol Genet Metab Rep, 9, 98-105.
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining