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Published in 2017 at "BMJ Open"
DOI: 10.1136/bmjopen-2016-014410
Abstract: Objective Mucopolysaccharidosis (MPS) IVA (Morquio syndrome A) is an autosomal-recessive lysosomal storage disorder caused by the deficiency of N-acetylgalactosamine-6-sulfatase (GALNS) resulting in excessive lysosomal storage of keratan sulfate. Treatments for MPS IVA have recently become…
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Keywords:
bio plex;
mps iva;
galns;
plex immunoassay ... See more keywords