Abnormal transport along the lysosomal pathway in Mucolipidosis, type IV disease
Mucolipidosis, type IV (ML-IV) is an autosomal recessive storage disease that is characterized by lysosomal accumulation of sphingolipids, phospholipids, and acid mucopolysaccharides. Unlike most other storage diseases, the lysosomal hydrolases participating in the catabolism of the stored molecules...
Na minha lista:
| Publicado no: | Proc Natl Acad Sci U S A |
|---|---|
| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1998
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC27719/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9600972/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.11.6373 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|