ENZYMES IN A GLYCOGEN STORAGE MYOPATHY.

@article{Larner1959ENZYMESIA,
  title={ENZYMES IN A GLYCOGEN STORAGE MYOPATHY.},
  author={J. Larner and C. Villar-Palasi},
  journal={Proceedings of the National Academy of Sciences of the United States of America},
  year={1959},
  volume={45 8},
  pages={
          1234-5
        }
}
  • J. Larner, C. Villar-Palasi
  • Published 1959
  • Chemistry, Medicine
  • Proceedings of the National Academy of Sciences of the United States of America
McArdle has reported a "myopathy due to a defect in muscle glycogen breakdown"' which appears to be a type of glycogen storage disease distinct from the previously reported classes.2 Schmid and Mahler' using muscle homogenates from a patient similar to the one described by McArdle have found that lactate is formed from added glucose 1-phosphate at a rate comparable to that of controls, but addition of muscle glycogen did not increase production of lactate. The content of glycogen in the muscles… Expand
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PHOSPHORYLASE AND RELATED ENZYMES OF GLYCOGEN METABOLISM.
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References

Phosphorus Metabolism II, ed
  • Polysaccharides
  • 1959