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Proteomic analysis of muccopolysaccharidosis I mouse brain with two-dimensional polyacrylamide gel electrophoresis
Mucopolysaccharidosis type I (MPS I) is due to deficiency of α-L-iduronidase (IDUA) and subsequent storage of undegraded glycosaminoglycans (GAG). The severe form of the disease, known as Hurler syndrome, is characterized by mental retardation and neurodegeneration of unknown etiology. To identify p...
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| Publicado en: | Mol Genet Metab |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5293606/ https://ncbi.nlm.nih.gov/pubmed/27742266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.10.001 |
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