Characterization of a canine model of glycogen storage disease type IIIa

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 model fo...

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Autores principales: Yi, Haiqing, Thurberg, Beth L., Curtis, Sarah, Austin, Stephanie, Fyfe, John, Koeberl, Dwight D., Kishnani, Priya S., Sun, Baodong
Formato: Artigo
Lenguaje:Inglês
Publicado: The Company of Biologists Limited 2012
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3484863/
https://ncbi.nlm.nih.gov/pubmed/22736456
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.009712
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