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Biomarkers in Glycogen Storage Diseases: An Update

Glycogen storage diseases (GSDs) are a group of 19 hereditary diseases caused by a lack of one or more enzymes involved in the synthesis or degradation of glycogen and are characterized by deposits or abnormal types of glycogen in tissues. Their frequency is very low and they are considered rare dis...

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Bibliografiske detaljer
Udgivet i:Int J Mol Sci
Main Authors: Molares-Vila, Alberto, Corbalán-Rivas, Alberte, Carnero-Gregorio, Miguel, González-Cespón, José Luís, Rodríguez-Cerdeira, Carmen
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2021
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8122709/
https://ncbi.nlm.nih.gov/pubmed/33922238
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22094381
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