Postnatal progression of bone disease in the cervical spines of mucopolysaccharidosis I dogs

INTRODUCTION: Mucopolysaccharidosis I (MPS I) is a lysosomal storage disorder characterized by deficient α-L-iduronidase activity leading to accumulation of poorly degraded dermatan and heparan sulfate glycosaminoglycans (GAGs). MPS I is associated with significant cervical spine disease, including...

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Bibliografiska uppgifter
Huvudupphovsmän: Chiaro, Joseph A, Baron, Matthew D, del Alcazar, Chelsea, O’Donnell, Patricia, Shore, Eileen M, Elliott, Dawn M, Ponder, Katherine P, Haskins, Mark E, Smith, Lachlan J
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3668665/
https://ncbi.nlm.nih.gov/pubmed/23563357
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2013.03.014
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