Mucopolysaccharidosis VI

Mucopolysaccharidosis VI (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B leading to the accumulation of dermatan sulfate. Birth prevalence is between 1 in 43,261 and 1 in 1,505,160 live births. The disorder shows a wid...

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Detalles Bibliográficos
Autores principales: Valayannopoulos, Vassili, Nicely, Helen, Harmatz, Paul, Turbeville, Sean
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873242/
https://www.ncbi.nlm.nih.gov/pubmed/20385007
http://dx.doi.org/10.1186/1750-1172-5-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873242/
https://www.ncbi.nlm.nih.gov/pubmed/20385007
http://dx.doi.org/10.1186/1750-1172-5-5

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