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An in silico approach to identify early damage biomarker candidates in metachromatic leukodystrophy
Metachromatic leukodystrophy (MLD) is a rare, autosomal recessive lysosomal storage disease. Deficient activity of arylsulfatase A causes sulfatides to accumulate in cells of different tissues, including those in the central and peripheral nervous systems, leading to progressive demyelination and ne...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233284/ https://www.ncbi.nlm.nih.gov/pubmed/37275681 http://dx.doi.org/10.1016/j.ymgmr.2023.100974 |