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Arterial Pathology in Canine Mucopolysaccharidosis-I and Response to Therapy
Mucopolysaccharidosis-I (MPS-I) is an inherited deficiency of α-L-iduronidase (IdU) that causes lysosomal accumulation of glycosaminoglycans (GAG) in a variety of parenchymal cell types and connective tissues. The fundamental link between genetic mutation and tissue GAG accumulation is clear, but re...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084338/ https://www.ncbi.nlm.nih.gov/pubmed/21383673 http://dx.doi.org/10.1038/labinvest.2011.7 |