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Recent development and gene therapy for glycogen storage disease type Ia
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive metabolic disorder caused by a deficiency in glucose-6-phosphatase-α (G6Pase-α or G6PC) that is expressed primarily in the liver, kidney, and intestine. G6Pase-α catalyzes the hydrolysis of glucose-6-phosphate (G6P) to glucose and p...
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| Publicado no: | Liver Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5859325/ https://ncbi.nlm.nih.gov/pubmed/29576889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.livres.2017.12.001 |
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