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    Structural and biochemical studies on Pompe disease and a “pseudodeficiency of acid α-glucosidase”

    We constructed structural models of the catalytic domain and the surrounding region of human wild-type acid α-glucosidase and the enzyme with amino acid substitutions by means of homology modeling, and examine...

    Youichi Tajima, Fumiko Matsuzawa, Sei-ichi Aikawa… in Journal of Human Genetics (2007)

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