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Published in 2021 at "Pakistan Journal of Medical Sciences"
DOI: 10.12669/pjms.37.3.2930
Abstract: Background and Objectives: Gaucher disease (GD) is a rare hereditary disorder caused by deficiency of the lysosomal enzyme β-glucocerebrosidase. An early and definitive diagnosis minimizes the sequelae of misdiagnoses, and unnecessary and invasive diagnostic procedures.…
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Keywords:
diagnosis gaucher;
gaucher disease;
disease;
disease iraq ... See more keywords