Fenofibrate rapidly decreases hepatic lipid and glycogen storage in neonatal mice with glycogen storage disease type Ia

Glycogen storage disease type Ia (GSD Ia) is caused by autosomal mutations in glucose-6-phosphatase α catalytic subunit (G6PC) and can present with severe hypoglycemia, lactic acidosis and hypertriglyceridemia. In both children and adults with GSD Ia, there is over-accumulation of hepatic glycogen a...

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Pubblicato in:Hum Mol Genet
Autori principali: Yavarow, Zollie A, Kang, Hye-Ri, Waskowicz, Lauren R, Bay, Boon-Huat, Young, Sarah P, Yen, Paul M, Koeberl, Dwight D
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2020
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General Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7003036/
https://ncbi.nlm.nih.gov/pubmed/31816064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz290
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