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- W2896780413 abstract "Type III glycogen storage disease (GSD-III) is an autosomal recessive disorder due to the deficiency of the glycogen debrancher enzyme. 80% of the patients have hepatic and muscular involvement (IIIa), compared to 15% with only liver involvement (IIIb). As the life expectancy improves in these patients, the possible liver complications are better understood." @default.
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- W2896780413 date "2018-01-01" @default.
- W2896780413 modified "2023-10-18" @default.
- W2896780413 title "Liver transplantation in patients with type IIIa glycogen storage disease, cirrhosis and hepatocellular carcinoma" @default.
- W2896780413 doi "https://doi.org/10.17235/reed.2018.5856/2018" @default.
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- W2896780413 hasPublicationYear "2018" @default.
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