The characterisation of pulmonary function in patients with mucopolysaccharidoses IVA: A longitudinal analysis

INTRODUCTION: Mucopolysaccharidosis (MPS) type IVA is a rare, autosomal recessive lysosomal storage disease causing substrate accumulation in various organs and tissues. MPS IVA is associated with both obstructive and restrictive airway disease, with the former often resulting in sleep disordered br...

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Detalles Bibliográficos
Autores principales: Kenth, Johnny J., Thompson, Gabrielle, Fullwood, Catherine, Wilkinson, Stuart, Jones, Simon, Bruce, I.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629586/
https://www.ncbi.nlm.nih.gov/pubmed/31341787
http://dx.doi.org/10.1016/j.ymgmr.2019.100487

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629586/
https://www.ncbi.nlm.nih.gov/pubmed/31341787
http://dx.doi.org/10.1016/j.ymgmr.2019.100487

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