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Cardiac manifestations in the mouse model of mucopolysaccharidosis I
Mucopolysaccharidosis I (MPS I, α-l-iduronidase deficiency disease) is a heritable lysosomal storage disorder involving multiple organs, including the heart. Malfunction of the heart is also a major manifestation in the mouse model of MPS I, progressing in severity from 6 to 10 months (of a one-year...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1369003/ https://ncbi.nlm.nih.gov/pubmed/15979918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2005.05.003 |
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