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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...

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Detalles Bibliográficos
Autores principales:	Abdulkarim, Haya, Siaj, Mohamed
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2022
Materias:	Article
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

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