Progression of Vertebral Bone Disease in Mucopolysaccharidosis VII Dogs from Birth to Skeletal Maturity

Mucopolysaccharidosis (MPS) VII is a lysosomal storage disorder characterized by deficient β-glucuronidase activity, leading to accumulation of incompletely degraded heparan, dermatan and chondroitin sulfate glycosaminoglycans. Patients with MPS VII exhibit progressive spinal deformity, which decrea...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Mol Genet Metab
Päätekijät: Peck, Sun H., Lau, Yian Khai, Kang, Jennifer L., Lin, Megan, Arginteanu, Toren, Matalon, Dena R., Bendigo, Justin R., O’Donnell, Patricia, Haskins, Mark E., Casal, Margret L., Smith, Lachlan J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2021
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8289741/
https://ncbi.nlm.nih.gov/pubmed/34154922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2021.06.005
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