Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders, characterized by the deficiency/absence of one of the enzymes involved in the intralysosomal degradation of glycosaminoglycans (GAGs). The quantitative determination of urinary GAGs using dimethylmethylene blue (DMB) shows high
โฆ LIBER โฆ
Adjunctive tests for the mucopolysaccharidoses
โ Scribed by Sally Kelly
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 115 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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