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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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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Company of Biologists Limited
2012
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| Témata: | |
| On-line přístup: | 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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