Characterization of a canine model of glycogen storage disease type IIIa

SUMMARY Glycogen storage disease type IIIa (GSD IIIa) is an autosomal recessive disease caused by deficiency of glycogen debranching enzyme (GDE) in liver and muscle. The disorder is clinically heterogeneous and progressive, and there is no effective treatment. Previously, a naturally occurring dog...

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Main Authors: Haiqing Yi (Author), Beth L. Thurberg (Author), Sarah Curtis (Author), Stephanie Austin (Author), John Fyfe (Author), Dwight D. Koeberl (Author), Priya S. Kishnani (Author), Baodong Sun (Author)
Format: Book
Published: The Company of Biologists, 2012-11-01T00:00:00Z.
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