Surgical Management of Spinal Disorders in People with Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are a group of inherited, multisystem, lysosomal storage disorders involving specific lysosomal enzyme deficiencies that result in the accumulation of glycosaminoglycans (GAG) secondary to insufficient degradation within cell lysosomes. GAG accumulation affects both prima...

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Detalles Bibliográficos
Autores principales: Terai, Hidetomi, Nakamura, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037985/
https://www.ncbi.nlm.nih.gov/pubmed/32050679
http://dx.doi.org/10.3390/ijms21031171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037985/
https://www.ncbi.nlm.nih.gov/pubmed/32050679
http://dx.doi.org/10.3390/ijms21031171

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