A glycogen storage disease type 1a patient with type 2 diabetes
Abstract Background Glycogen storage disease type 1a (GSD1a) is an inborn genetic disease caused by glucose-6-phosphatase-α (G6Pase-α) deficiency and is often observed to lead to endogenous glucose production disorders manifesting as hypoglycemia, hyperuricemia, hyperlipidemia, lactic acidemia, hepa...
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Main Authors: | , , , , , , |
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Format: | Book |
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BMC,
2022-09-01T00:00:00Z.
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A1234.567 |
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