Gaucher Disease (GD) is a rare, inherited lysosomal storage disorder (LSD) that is classified into three forms - Types 1, 2, and 3 - which are distinguished by their symptoms, severity, and neurological involvement. GD affects the ability of cells to break down a specific type of fat, glucocerebroside (GC), as a result of the deficiency or limited activity of the enzyme glucocerebrosidase (GCase). Browse Full Report With TOC @ http://www.researchmoz.us/epicast-report-gaucher-disease-epidemiology-forecast-to-2024-report.html
http://www.researchmoz.us/epicast-report-gaucher-disease-epidemiology-forecast-to-2024-report.html
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