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Label-free multiplex electrochemical immunosensor for early diagnosis of lysosomal storage disorders
Pompe, Gaucher and Krabbe disease are lysosomal storage disorders (LSDs) which are a group of genetic diseases that causes the accumulation of lipids in tissues and cells. Pompe, Gaucher and Krabbe are characterized by the deficiency of acid α-glucosidase (GAA), β-Glucocerebrosidase (GBA) and galact...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167275/ https://www.ncbi.nlm.nih.gov/pubmed/35662258 http://dx.doi.org/10.1038/s41598-022-13259-1 |