Quantitation of a Urinary Profile of Biomarkers in Gaucher Disease Type 1 Patients Using Tandem Mass Spectrometry
Gaucher disease is a rare inherited disorder caused by a deficiency of the lysosomal acid beta-glucocerebrosidase enzyme. Metabolomic studies by our group targeted several new potential urinary biomarkers. Apart from lyso-Gb<sub>1</sub>, these studies highlighted lyso-Gb<sub>1</sub> analogs −28, −26...
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| Principais autores: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2022-06-01
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| coleção: | Diagnostics |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2075-4418/12/6/1414 |
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