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: Yi Sun (Author), Wenhui Qiang (Author), Runze Wu (Author), Tong Yin (Author), Jie Yuan (Author), Jin Yuan (Author), Yunjuan Gu (Author)
Format: Book
Published: BMC, 2022-09-01T00:00:00Z.
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3rd Floor Main Library

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