A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0
<p>Abstract</p> <p>Background</p> <p>Glycogen storage disease type 0 is an autosomal recessive disease presenting in infancy or early childhood and characterized by ketotic hypoglycemia after prolonged fasting and postprandial hyperglycemia and hyperlactatemia. Sixteen...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2010-01-01T00:00:00Z.
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