New approaches in the diagnosis of lysosomal storage disorders based on the determination of free oligosaccha- rides in urine
Marek Nemčovič, Zuzana Pakanová, Anna Šalingová, Claudia Šebová, Mária Ostrožlíková, Ján Mucha
The diagnosis of lysosomal storage disorders requires a highly personalized approach as these diseases cov- er a wide range of hereditary metabolic disorders with highly...
diagnostics, glycogenoses, lysosomal storage disorders, MALDI TOF/TOF
newsLab 2020, 1 : 24-26
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